A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745979



Internal ID18697574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52726879..52807526hg38UCSC Ensembl
Innerchr5:52022713..52103360hg19UCSC Ensembl
Innerchr5:52058470..52139117hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3880648
hg1980648
hg1880648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027410
Supporting Variants
Samples
Known GenesITGA1, PELO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3745979
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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