A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3474136



Internal ID19065830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79075272..79154040hg38UCSC Ensembl
Innerchr1:79540957..79619725hg19UCSC Ensembl
Innerchr1:79313545..79392313hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3878769
hg1978769
hg1878769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007013
Supporting Variants
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)nssv3474136
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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