A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701171



Internal ID15437823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:55081026..55411823hg38UCSC Ensembl
Innerchr3:55115053..55445851hg19UCSC Ensembl
Innerchr3:55090093..55420891hg18UCSC Ensembl
Innerchr3:55090093..55420891hg17UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38330798
hg19330799
hg18330799
hg17330799
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525110
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701171
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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