A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613136



Internal ID16400545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2495675..2515607hg38UCSC Ensembl
Innerchr9:2495675..2515607hg19UCSC Ensembl
Innerchr9:2485675..2505607hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3819933
hg1919933
hg1819933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126220
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613136
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