A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032497



Internal ID18775031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172660175..172726439hg38UCSC Ensembl
Innerchr5:172087178..172153442hg19UCSC Ensembl
Innerchr5:172019783..172086047hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3866265
hg1966265
hg1866265
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649141
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)nsv1032497
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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