A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549926



Internal ID16337335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6635805..6788775hg38UCSC Ensembl
Innerchr10:6677767..6830737hg19UCSC Ensembl
Innerchr10:6717773..6870743hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38152971
hg19152971
hg18152971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv951n54
Supporting Variantsnssv1174117
SamplesHGDP00970
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549926
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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