A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528776



Internal ID15109383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:54471593..54740381hg38UCSC Ensembl
Innerchr18:51997963..52407612hg19UCSC Ensembl
Innerchr18:50251961..50558610hg18UCSC Ensembl
Innerchr18:50251961..50558610hg17UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38268789
hg19409650
hg18306650
hg17306650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv188n21
Supporting Variantsnssv705441
Samples
Known GenesDYNAP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528776
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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