A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746634



Internal ID18698229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:125059125..125095527hg38UCSC Ensembl
Innerchr5:124394818..124431220hg19UCSC Ensembl
Innerchr5:124422717..124459119hg18UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3836403
hg1936403
hg1836403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019740
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)nssv3746634
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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