A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv709202



Internal ID15656472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6384304..6385638hg38UCSC Ensembl
Innerchr1:6444364..6445698hg19UCSC Ensembl
Innerchr1:6366951..6368285hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381335
hg191335
hg181335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545255
Supporting Variants
Samples
Known GenesACOT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv709202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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