A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662080



Internal ID15052046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:195629044..195671781hg38UCSC Ensembl
Innerchr2:196493768..196536505hg19UCSC Ensembl
Innerchr2:196202013..196244750hg18UCSC Ensembl
Innerchr2:196319274..196362011hg17UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3842738
hg1942738
hg1842738
hg1742738
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515614
Supporting Variants
Samples
Known GenesSLC39A10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662080
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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