A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704767



Internal ID15441419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:64174453..64186078hg38UCSC Ensembl
Innerchr3:64160129..64171754hg19UCSC Ensembl
Innerchr3:64135169..64146794hg18UCSC Ensembl
Innerchr3:64135169..64146794hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3811626
hg1911626
hg1811626
hg1711626
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528206
Supporting Variants
Samples
Known GenesPRICKLE2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704767
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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