A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669282



Internal ID15405934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75379524..75481744hg38UCSC Ensembl
Innerchr3:75428675..75530895hg19UCSC Ensembl
Innerchr3:75511365..75613585hg18UCSC Ensembl
Innerchr3:75511365..75613585hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38102221
hg19102221
hg18102221
hg17102221
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517173
Supporting Variants
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669282
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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