A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666743



Internal ID15056709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8051071..8056756hg38UCSC Ensembl
Innerchr10:8093034..8098719hg19UCSC Ensembl
Innerchr10:8133040..8138725hg18UCSC Ensembl
Innerchr10:8133040..8138725hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385686
hg195686
hg185686
hg175686
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517198
Supporting Variants
Samples
Known GenesGATA3, GATA3-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666743
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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