A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545926



Internal ID16333335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:30081837..30705816hg38UCSC Ensembl
Innerchr1:30554684..31178663hg19UCSC Ensembl
Innerchr1:30327271..30951250hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38623980
hg19623980
hg18623980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv221n54
Supporting Variantsnssv712057
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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