A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv745565



Internal ID16039521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28371674..28375869hg38UCSC Ensembl
Innerchr10:28660603..28664798hg19UCSC Ensembl
Innerchr10:28700609..28704804hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg384196
hg194196
hg184196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550291
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)nssv745565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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