A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614356



Internal ID16401765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42457621..42458697hg38UCSC Ensembl
Innerchr9:43353497..43354573hg19UCSC Ensembl
Innerchr9:43293493..43294569hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381077
hg191077
hg181077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12704n54
Supporting Variantsnssv1134248, nssv1134272, nssv1134237, nssv1134263, nssv1134254, nssv1134269, nssv1134270, nssv1134259, nssv1134247, nssv1134256, nssv1134246, nssv1134242, nssv1134244, nssv1134257, nssv1134261, nssv1134251, nssv1134260, nssv1134264, nssv1134255, nssv1134240, nssv1134238, nssv1134267, nssv1134258, nssv1134234, nssv1134245, nssv1134273, nssv1134243, nssv1134239, nssv1134253, nssv1134235, nssv1134252, nssv1134265, nssv1134249, nssv1134266, nssv1134271, nssv1134241, nssv1134262, nssv1134250, nssv1134236, nssv1134268
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614356
Frequency
Sample Size17421
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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