A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614729



Internal ID16055452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77291835..77366058hg38UCSC Ensembl
Innerchr9:79906751..79980974hg19UCSC Ensembl
Innerchr9:79096571..79170794hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3874224
hg1974224
hg1874224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176454
SamplesHGDP00292
Known GenesVPS13A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614729
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer