A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016535



Internal ID18759070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172653521..172735933hg38UCSC Ensembl
Innerchr5:172080524..172162936hg19UCSC Ensembl
Innerchr5:172013129..172095541hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3882413
hg1982413
hg1882413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5831n100
Supporting Variantsnssv3746672, nssv3649135, nssv3649134
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)nsv1016535
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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