A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007013



Internal ID19096231
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 StatusM
Merged Variantsdgv202n100
Supporting Variantsnssv3474136
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)nsv1007013
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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