A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615377



Internal ID16402786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127846017..127854679hg38UCSC Ensembl
Innerchr9:130608296..130616958hg19UCSC Ensembl
Innerchr9:129648117..129656779hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg388663
hg198663
hg188663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141633
Samples
Known GenesENG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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