A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653991



Internal ID15043957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8044207..8056756hg38UCSC Ensembl
Innerchr10:8086170..8098719hg19UCSC Ensembl
Innerchr10:8126176..8138725hg18UCSC Ensembl
Innerchr10:8126176..8138725hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3812550
hg1912550
hg1812550
hg1712550
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)nssv653991
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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