A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv762176



Internal ID16056132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133123890..133189333hg38UCSC Ensembl
Innerchr10:134937394..135002837hg19UCSC Ensembl
Innerchr10:134787384..134852827hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3865444
hg1965444
hg1865444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552569
Supporting Variants
Samples
Known GenesGPR123, KNDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv762176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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