A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027773



Internal ID19116991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:23644670..23776269hg38UCSC Ensembl
Innerchr6:23644898..23776497hg19UCSC Ensembl
Innerchr6:23752877..23884476hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38131600
hg19131600
hg18131600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654832
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027773
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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