A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615742



Internal ID16403151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133942648..133970221hg38UCSC Ensembl
Innerchr9:136807770..136835343hg19UCSC Ensembl
Innerchr9:135797591..135825164hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3827574
hg1927574
hg1827574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176369
Samples1780862345_A
Known GenesVAV2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615742
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