A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591935



Internal ID16379344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145604180..145673313hg38UCSC Ensembl
Innerchr3:145321967..145391100hg19UCSC Ensembl
Innerchr3:146804657..146873790hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3869134
hg1969134
hg1869134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152551
Samples1780854491_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591935
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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