A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693785



Internal ID15430437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132013576..132021336hg38UCSC Ensembl
Innerchr3:131732420..131740180hg19UCSC Ensembl
Innerchr3:133215110..133222870hg18UCSC Ensembl
Innerchr3:133215118..133222878hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg387761
hg197761
hg187761
hg177761
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517016
Supporting Variants
Samples
Known GenesCPNE4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693785
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer