A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696070



Internal ID15086036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11018310..11024121hg38UCSC Ensembl
Innerchr3:11059996..11065807hg19UCSC Ensembl
Innerchr3:11034996..11040807hg18UCSC Ensembl
Innerchr3:11034996..11040807hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg385812
hg195812
hg185812
hg175812
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518622
Supporting Variants
Samples
Known GenesSLC6A1, SLC6A1-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696070
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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