A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv743993



Internal ID15691263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8032474..8074635hg38UCSC Ensembl
Innerchr10:8074437..8116598hg19UCSC Ensembl
Innerchr10:8114443..8156604hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3842162
hg1942162
hg1842162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549949
Supporting Variants
Samples
Known GenesGATA3, GATA3-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv743993
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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