A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703497



Internal ID15093463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28217948..28218776hg38UCSC Ensembl
Innerchr6:28185726..28186554hg19UCSC Ensembl
Innerchr6:28293705..28294533hg18UCSC Ensembl
Innerchr6:28293705..28294533hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38829
hg19829
hg18829
hg17829
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527115
Supporting Variants
Samples
Known GenesTOB2P1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703497
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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