A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527224



Internal ID15454517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189831634..189833631hg38UCSC Ensembl
Innerchr3:189549423..189551420hg19UCSC Ensembl
Innerchr3:191032117..191034114hg18UCSC Ensembl
Innerchr3:191032125..191034122hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381998
hg191998
hg181998
hg171998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703624
Samples
Known GenesTP63
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527224
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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