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Human Genome Region REGION69

Assembly:
GRCh37.p13
Location:
chr17:77,412,077-77,766,016
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-748 Resolved Reference Assembly gap between AC142247.2 and AC027824.17 AC233701.6 has been sequenced and submitted and closes this gap.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH591186.1 NW_003871089.1 FIX 376,223 280 106,481
           

REGION69 -- chr17 (NC_000017.10):77,412,077-77,766,016