A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv715269



Internal ID16009225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58903275..58992143hg38UCSC Ensembl
Innerchr1:59368947..59457815hg19UCSC Ensembl
Innerchr1:59141535..59230403hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3888869
hg1988869
hg1888869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546316
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)nssv715269
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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