A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549928



Internal ID16337337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6635805..6795823hg38UCSC Ensembl
Innerchr10:6677767..6837785hg19UCSC Ensembl
Innerchr10:6717773..6877791hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38160019
hg19160019
hg18160019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv951n54
Supporting Variantsnssv743553
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549928
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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