A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615525



Internal ID16056248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130486627..130518123hg38UCSC Ensembl
Innerchr9:133362014..133393510hg19UCSC Ensembl
Innerchr9:132351835..132383331hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3831497
hg1931497
hg1831497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12911n54
Supporting Variantsnssv1145191
Samples
Known GenesASS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615525
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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