A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614961



Internal ID16402370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101132879..101160903hg38UCSC Ensembl
Innerchr9:103895161..103923185hg19UCSC Ensembl
Innerchr9:102934982..102963006hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3828025
hg1928025
hg1828025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176004
Samples1782681287_A
Known GenesLPPR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614961
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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