A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174117



Internal ID15877336
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 StatusS
Merged Variantsnsv549926
Supporting Variants
SamplesHGDP00970
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174117
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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