A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682937



Internal ID15072903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149823865..150090941hg38UCSC Ensembl
Innerchr6:150145001..150412077hg19UCSC Ensembl
Innerchr6:150186694..150453770hg18UCSC Ensembl
Innerchr6:150237115..150504191hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38267077
hg19267077
hg18267077
hg17267077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517022
Supporting Variants
Samples
Known GenesLRP11, RAET1E, RAET1E-AS1, RAET1G, RAET1K, RAET1L, ULBP1, ULBP2, ULBP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682937
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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