A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746557



Internal ID19044838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109881727..109942456hg38UCSC Ensembl
Innerchr5:109217428..109278157hg19UCSC Ensembl
Innerchr5:109245327..109306056hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3860730
hg1960730
hg1860730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016715
Supporting Variants
Samples
Known GenesLOC100289673
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3746557
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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