A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526832



Internal ID15107439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73563798..74732599hg38UCSC Ensembl
Innerchr3:73612949..74781750hg19UCSC Ensembl
Innerchr3:73695639..74864440hg18UCSC Ensembl
Innerchr3:73695639..74864440hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381168802
hg191168802
hg181168802
hg171168802
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703189
Samples
Known GenesCNTN3, PDZRN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526832
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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