A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746157



Internal ID18697752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3572260..3678663hg38UCSC Ensembl
Innerchr5:3572374..3678777hg19UCSC Ensembl
Innerchr5:3625374..3731777hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38106404
hg19106404
hg18106404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029309
Supporting Variants
Samples
Known GenesIRX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3746157
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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