A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614949



Internal ID16402358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98565918..98599302hg38UCSC Ensembl
Innerchr9:101328200..101361584hg19UCSC Ensembl
Innerchr9:100368021..100401405hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3833385
hg1933385
hg1833385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140212
Samples
Known GenesGABBR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614949
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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