A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051656



Internal ID15558156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28449445..28606638hg38UCSC Ensembl
Innerchr6:28417222..28574415hg19UCSC Ensembl
Innerchr6:28525201..28682394hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38157194
hg19157194
hg18157194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601210
Supporting Variants
Samples
Known GenesGPX5, GPX6, SCAND3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051656
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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