A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525688



Internal ID15452981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:234889828..234891924hg38UCSC Ensembl
Innerchr1:235025575..235027671hg19UCSC Ensembl
Innerchr1:233092198..233094294hg18UCSC Ensembl
Innerchr1:231332310..231334406hg17UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382097
hg192097
hg182097
hg172097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701846
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525688
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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