A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057787



Internal ID15564287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33964665..34227234hg38UCSC Ensembl
Innerchr6:33932442..34195011hg19UCSC Ensembl
Innerchr6:34040420..34302989hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38262570
hg19262570
hg18262570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602843
Supporting Variants
Samples
Known GenesGRM4, MIR1275
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057787
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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