A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746660



Internal ID19044941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163318463..163373592hg38UCSC Ensembl
Innerchr5:162745469..162800598hg19UCSC Ensembl
Innerchr5:162678047..162733176hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3855130
hg1955130
hg1855130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022560
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3746660
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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