A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614851



Internal ID16402260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89675959..89725009hg38UCSC Ensembl
Innerchr9:92290874..92339924hg19UCSC Ensembl
Innerchr9:91480694..91529744hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3849051
hg1949051
hg1849051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176365
Samples1780862345_A
Known GenesUNQ6494
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614851
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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