A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154281



Internal ID15533622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31489801hg38UCSC Ensembl
Innerchr6:31360389..31457578hg19UCSC Ensembl
Innerchr6:31468368..31565557hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3897190
hg1997190
hg1897190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601903
Supporting Variants
SamplesNINDS_192
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154281
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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