A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712050



Internal ID15659320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28237768..28323866hg38UCSC Ensembl
Innerchr1:28564279..28650377hg19UCSC Ensembl
Innerchr1:28436866..28522964hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3886099
hg1986099
hg1886099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545917
Supporting Variants
Samples
Known GenesATPIF1, SESN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712050
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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