A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690137



Internal ID15080103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:13798450..13828347hg38UCSC Ensembl
Innerchr5:13798559..13828456hg19UCSC Ensembl
Innerchr5:13851559..13881456hg18UCSC Ensembl
Innerchr5:13851559..13881456hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3829898
hg1929898
hg1829898
hg1729898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516415
Supporting Variants
Samples
Known GenesDNAH5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690137
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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