A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057882



Internal ID15911068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34236610..34238257hg38UCSC Ensembl
Innerchr6:34204387..34206034hg19UCSC Ensembl
Innerchr6:34312365..34314012hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381648
hg191648
hg181648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602871
Supporting Variants
Samples
Known GenesHMGA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057882
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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