A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673246



Internal ID15063212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149823865..150095595hg38UCSC Ensembl
Innerchr6:150145001..150416731hg19UCSC Ensembl
Innerchr6:150186694..150458424hg18UCSC Ensembl
Innerchr6:150237115..150508845hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38271731
hg19271731
hg18271731
hg17271731
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)nssv673246
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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