A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525829



Internal ID15106436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145896530..146145992hg38UCSC Ensembl
Innerchr3:145614317..145863779hg19UCSC Ensembl
Innerchr3:147097007..147346469hg18UCSC Ensembl
Innerchr3:147097015..147346477hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38249463
hg19249463
hg18249463
hg17249463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702018
Samples
Known GenesPLOD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525829
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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