A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525195



Internal ID15452488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59070555..59077434hg38UCSC Ensembl
Innerchr18:56737787..56744666hg19UCSC Ensembl
Innerchr18:54888767..54895646hg18UCSC Ensembl
Innerchr18:54888767..54895646hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg386880
hg196880
hg186880
hg176880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701276
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525195
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer