A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635968



Internal ID18934249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27458492..27501922hg38UCSC Ensembl
Innerchr5:27458599..27502029hg19UCSC Ensembl
Innerchr5:27494356..27537786hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3843431
hg1943431
hg1843431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030914
Supporting Variants
Samples
Known GenesLINC01021
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635968
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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