A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527064



Internal ID15454357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:203240353..203271176hg38UCSC Ensembl
Innerchr1:203209481..203240304hg19UCSC Ensembl
Innerchr1:201476104..201506927hg18UCSC Ensembl
Innerchr1:199941138..199971961hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3830824
hg1930824
hg1830824
hg1730824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703443
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527064
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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