A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668023



Internal ID15057989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110420408..110426546hg38UCSC Ensembl
Innerchr6:110741611..110747749hg19UCSC Ensembl
Innerchr6:110848304..110854442hg18UCSC Ensembl
Innerchr6:110848304..110854442hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386139
hg196139
hg186139
hg176139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516397
Supporting Variants
Samples
Known GenesSLC22A16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668023
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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