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CRA_TCAGchr7v1

Organism name:
Homo sapiens (human)
BioProject:
PRJNA10793
Submitter:
The Centre for Applied Genomics
Date:
2003/04/11
Assembly level:
Chromosome
Genome representation:
partial
Excluded from RefSeq:
  • partial
GenBank assembly accession:
GCA_000002135.1 (replaced)
RefSeq assembly accession:
GCF_000002135.1 (suppressed) see latest RefSeq assemblies for this species
RefSeq assembly and GenBank assembly identical:
no (hide details)
  • Only in GenBank: chromosome 7
  • Data displayed for GenBank version
WGS Project:
AACC01

IDs: 4348 [UID] 294378 [GenBank] 4348 [RefSeq]

See Genome Information for Homo sapiens

Pathogen Detection Resources

There are 1094 assemblies for this organism

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History (Show revision history)

Comment

Global statistics

Total sequence length157,953,789
Total ungapped length154,833,105
Gaps between scaffolds7
Number of scaffolds8
Scaffold N5054,358,329
Scaffold L502
Number of contigs146
Contig N503,664,911
Contig L5012
Total number of chromosomes and plasmids1
Number of component sequences (WGS or clone)235

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Assembly Information

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Global assembly definition

Download the full sequence report
Click on the table row to see sequence details in the table to the right
Assembly Unit Name
Primary Assembly
Assembly Unit: Primary Assembly (GCA_000000255.1)
Molecule nameGenBank sequenceRefSeq sequence
Chromosome 7BL000001.1n/an/a

Assembly statistics

MoleculeTotal
Length		Scaffold
Count		Ungapped
Length		Scaffold
N50		Spanned
Gaps		Unspanned
Gaps
Chromosome 7157,953,7898154,833,10554,358,3291387