A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649136



Internal ID18600731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172653521..172739244hg38UCSC Ensembl
Innerchr5:172080524..172166247hg19UCSC Ensembl
Innerchr5:172013129..172098852hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3885724
hg1985724
hg1885724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031020
Supporting Variants
Samples
Known GenesNEURL1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649136
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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