A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614352



Internal ID16401761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42457621..42458749hg38UCSC Ensembl
Innerchr9:43353445..43354573hg19UCSC Ensembl
Innerchr9:43293441..43294569hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381129
hg191129
hg181129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12704n54
Supporting Variantsnssv1134222, nssv1134221, nssv1134220
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614352
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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