A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746661



Internal ID19044942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163318463..163378839hg38UCSC Ensembl
Innerchr5:162745469..162805845hg19UCSC Ensembl
Innerchr5:162678047..162738423hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3860377
hg1960377
hg1860377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033825
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)nssv3746661
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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