A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613615



Internal ID16401024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12830071..12947239hg38UCSC Ensembl
Innerchr9:12830070..12947238hg19UCSC Ensembl
Innerchr9:12820070..12937238hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38117169
hg19117169
hg18117169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128717
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613615
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