A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv743994



Internal ID15691264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8053377..8057214hg38UCSC Ensembl
Innerchr10:8095340..8099177hg19UCSC Ensembl
Innerchr10:8135346..8139183hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383838
hg193838
hg183838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549950
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)nssv743994
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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