A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615394



Internal ID16402803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128688840..128689538hg38UCSC Ensembl
Innerchr9:131451119..131451817hg19UCSC Ensembl
Innerchr9:130490940..130491638hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38699
hg19699
hg18699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1143225, nssv1143227, nssv1143226
Samples
Known GenesSET
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615394
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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