A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv743555



Internal ID16037511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6635805..6803275hg38UCSC Ensembl
Innerchr10:6677767..6845237hg19UCSC Ensembl
Innerchr10:6717773..6885243hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38167471
hg19167471
hg18167471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549929
Supporting Variants
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv743555
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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