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Human Genome Region SH2B2

Assembly:
GRCh37.p11
Location:
chr7:101,718,951-102,072,447
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-115 Resolved Sequence is missing from NM_020979.2 (SH2B2) when aligned to the reference assembly, suggesting some sequence is missing from the assembly. This patch corrects a deletion found in GRCh37 chromosome NC_000007.13, in component AC005088.3, affecting GeneID: 10603 (SH2B2).
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL582968.1 NW_003571037.1 FIX 356,330 166 2,932
           

SH2B2 -- chr7 (NC_000007.13):101,718,951-102,072,447