A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695299



Internal ID15431951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45932086..45947351hg38UCSC Ensembl
Innerchr6:45899823..45915088hg19UCSC Ensembl
Innerchr6:46007801..46023066hg18UCSC Ensembl
Innerchr6:46007801..46023066hg17UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3815266
hg1915266
hg1815266
hg1715266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517891
Supporting Variants
Samples
Known GenesCLIC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695299
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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