A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615709



Internal ID16403118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133888124..133893464hg38UCSC Ensembl
Innerchr9:136753246..136758586hg19UCSC Ensembl
Innerchr9:135743067..135748407hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg385341
hg195341
hg185341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12949n54
Supporting Variantsnssv1146465
Samples
Known GenesVAV2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615709
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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