A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712059



Internal ID16006015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:30089416..30705816hg38UCSC Ensembl
Innerchr1:30562263..31178663hg19UCSC Ensembl
Innerchr1:30334850..30951250hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38616401
hg19616401
hg18616401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545928
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712059
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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