A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027494



Internal ID19116713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80064660..80131016hg38UCSC Ensembl
Innerchr7:79693976..79760332hg19UCSC Ensembl
Innerchr7:79531912..79598268hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3866357
hg1966357
hg1866357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655135
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)nsv1027494
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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