A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615708



Internal ID16403117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133888124..133892131hg38UCSC Ensembl
Innerchr9:136753246..136757253hg19UCSC Ensembl
Innerchr9:135743067..135747074hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg384008
hg194008
hg184008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12949n54
Supporting Variantsnssv1146464
Samples
Known GenesVAV2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615708
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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