A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523228



Internal ID15103835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59897033..59901461hg38UCSC Ensembl
Innerchr18:57564265..57568693hg19UCSC Ensembl
Innerchr18:55715245..55719673hg18UCSC Ensembl
Innerchr18:55715245..55719673hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg384429
hg194429
hg184429
hg174429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698951
Samples
Known GenesPMAIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523228
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