A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705257



Internal ID15095223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4613824..4731106hg38UCSC Ensembl
Innerchr6:4614058..4731340hg19UCSC Ensembl
Innerchr6:4559057..4676339hg18UCSC Ensembl
Innerchr6:4559057..4676339hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38117283
hg19117283
hg18117283
hg17117283
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528627
Supporting Variants
Samples
Known GenesCDYL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705257
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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