A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649124



Internal ID18947405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:169829996..169851112hg38UCSC Ensembl
Innerchr5:169257000..169278116hg19UCSC Ensembl
Innerchr5:169189578..169210694hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3821117
hg1921117
hg1821117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026577
Supporting Variants
Samples
Known GenesDOCK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649124
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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