A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528765



Internal ID15456058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:234917962..234926434hg38UCSC Ensembl
Innerchr1:235053709..235062181hg19UCSC Ensembl
Innerchr1:233120332..233128804hg18UCSC Ensembl
Innerchr1:231360444..231368916hg17UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg388473
hg198473
hg188473
hg178473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705428
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528765
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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