A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695134



Internal ID15431786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:64107187..64113893hg38UCSC Ensembl
Innerchr3:64092863..64099569hg19UCSC Ensembl
Innerchr3:64067903..64074609hg18UCSC Ensembl
Innerchr3:64067903..64074609hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg386707
hg196707
hg186707
hg176707
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522355
Supporting Variants
Samples
Known GenesPRICKLE2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695134
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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