A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv745568



Internal ID16039524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28371674..28376112hg38UCSC Ensembl
Innerchr10:28660603..28665041hg19UCSC Ensembl
Innerchr10:28700609..28705047hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg384439
hg194439
hg184439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550292
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)nssv745568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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