A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv715969



Internal ID15663239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61648509..61654137hg38UCSC Ensembl
Innerchr1:62114181..62119809hg19UCSC Ensembl
Innerchr1:61886769..61892397hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg385629
hg195629
hg185629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546392
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)nssv715969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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