A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522027



Internal ID15102634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:65160069..65167814hg38UCSC Ensembl
Innerchr1:65625752..65633497hg19UCSC Ensembl
Innerchr1:65398340..65406085hg18UCSC Ensembl
Innerchr1:65337773..65345518hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg387746
hg197746
hg187746
hg177746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694797
Samples
Known GenesAK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522027
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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