A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614327



Internal ID16401736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66844380..66865100hg38UCSC Ensembl
Innerchr9:40827741..40848459hg19UCSC Ensembl
Innerchr9:40817741..40838459hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3820721
hg1920719
hg1820719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134169, nssv1134173, nssv1134161, nssv1134168, nssv1134179, nssv1134164, nssv1134177, nssv1134165, nssv1134172, nssv1134178, nssv1134171, nssv1134160, nssv1134162, nssv1134175, nssv1134174, nssv1134163, nssv1134170, nssv1134176, nssv1134167, nssv1134166
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614327
Frequency
Sample Size17421
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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