A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703624



Internal ID15440276
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527224
Supporting Variants
Samples
Known GenesTP63
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703624
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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