A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712879



Internal ID15660149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:45034622..45161991hg38UCSC Ensembl
Innerchr1:45500294..45627663hg19UCSC Ensembl
Innerchr1:45272881..45400250hg18UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38127370
hg19127370
hg18127370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546148
Supporting Variants
Samples
Known GenesZSWIM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712879
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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