A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526339



Internal ID15453632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:72808804..72809002hg38UCSC Ensembl
Innerchr18:70476039..70476237hg19UCSC Ensembl
Innerchr18:68627019..68627217hg18UCSC Ensembl
Innerchr18:68627019..68627217hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38199
hg19199
hg18199
hg17199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702631
Samples
Known GenesNETO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526339
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