A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv762007



Internal ID16055963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111200..133111829hg38UCSC Ensembl
Innerchr10:134924704..134925333hg19UCSC Ensembl
Innerchr10:134774694..134775323hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38630
hg19630
hg18630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552549
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)nssv762007
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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