A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695556



Internal ID15432208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:64164530..64186078hg38UCSC Ensembl
Innerchr3:64150206..64171754hg19UCSC Ensembl
Innerchr3:64125246..64146794hg18UCSC Ensembl
Innerchr3:64125246..64146794hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3821549
hg1921549
hg1821549
hg1721549
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518137
Supporting Variants
Samples
Known GenesPRICKLE2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695556
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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