A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615967



Internal ID16403376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136510443..136598337hg38UCSC Ensembl
Innerchr9:139404895..139492789hg19UCSC Ensembl
Innerchr9:138524716..138612610hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3887895
hg1987895
hg1887895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148326
Samples
Known GenesMIR4673, MIR4674, NOTCH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615967
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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