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Human Genome Region SNTB2

Assembly:
GRCh37.p12
Location:
chr16:69,174,054-69,258,593
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1175 Resolved NOVEL patch GL383557.1 created to capture sequence from AC208009.3 not represented in reference chromosome NOVEL patch GL383557.1 created to capture 5141bp sequence from AC208009.3 not represented in reference chromosome
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383557.1 NW_003315946.1 NOVEL 89,672 35 5,160
           

SNTB2 -- chr16 (NC_000016.9):69,174,054-69,258,593