A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv743967



Internal ID15691237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7586456..8160993hg38UCSC Ensembl
Innerchr10:7628419..8202956hg19UCSC Ensembl
Innerchr10:7668425..8242962hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38574538
hg19574538
hg18574538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549933
Supporting Variants
Samples
Known GenesATP5C1, GATA3, GATA3-AS1, ITIH2, ITIH5, KIN, TAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv743967
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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