A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523567



Internal ID15450860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:32169615..32390967hg38UCSC Ensembl
Innerchr7:32209227..32430579hg19UCSC Ensembl
Innerchr7:32175752..32397104hg18UCSC Ensembl
Innerchr7:31982467..32203819hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38221353
hg19221353
hg18221353
hg17221353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699349
Samples
Known GenesPDE1C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523567
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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