A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615214



Internal ID16055937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113363509..113387687hg38UCSC Ensembl
Innerchr9:116125789..116149967hg19UCSC Ensembl
Innerchr9:115165610..115189788hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3824179
hg1924179
hg1824179
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141257
Samples
Known GenesALAD, BSPRY, HDHD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615214
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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