A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv761994



Internal ID16055950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111200..133111778hg38UCSC Ensembl
Innerchr10:134924704..134925282hg19UCSC Ensembl
Innerchr10:134774694..134775272hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38579
hg19579
hg18579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552548
Supporting Variants
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv761994
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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