A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526128



Internal ID15453421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173856727..174253013hg38UCSC Ensembl
Innerchr3:173574517..173970803hg19UCSC Ensembl
Innerchr3:175057211..175453497hg18UCSC Ensembl
Innerchr3:175057219..175453505hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38396287
hg19396287
hg18396287
hg17396287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv305n21
Supporting Variantsnssv702382
Samples
Known GenesNLGN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526128
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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