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Human Genome Region KRTAP_REGION_1

Assembly:
GRCh37.p13
Location:
chr17:39,006,985-39,589,187
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383564.1 NW_003315953.1 NOVEL 133,151 61 7,333
JH159146.1 NW_003871091.1 NOVEL 278,131 294 519
JH159147.1 NW_003871092.1 NOVEL 70,345 167 63
JH159148.1 NW_003871093.1 NOVEL 88,070 181 73
           

KRTAP_REGION_1 -- chr17 (NC_000017.10):39,006,985-39,589,187