A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526833



Internal ID15454126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:18048446..18051296hg38UCSC Ensembl
Innerchr1:18374940..18377790hg19UCSC Ensembl
Innerchr1:18247527..18250377hg18UCSC Ensembl
Innerchr1:18120246..18123096hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg382851
hg192851
hg182851
hg172851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703190
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526833
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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