A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551874



Internal ID16339283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89810454..90276397hg38UCSC Ensembl
Innerchr10:91570211..92036154hg19UCSC Ensembl
Innerchr10:91560191..92026134hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38465944
hg19465944
hg18465944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753328
Samples
Known GenesLINC00865
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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