A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700875



Internal ID15090841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10057112..10067286hg38UCSC Ensembl
Innerchr12:10209711..10219885hg19UCSC Ensembl
Innerchr12:10100978..10111152hg18UCSC Ensembl
Innerchr12:10100978..10111152hg17UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3810175
hg1910175
hg1810175
hg1710175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524870
Supporting Variants
Samples
Known GenesCLEC9A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700875
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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