A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527722



Internal ID15455015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:68746370..68857539hg38UCSC Ensembl
Innerchr1:69212053..69323222hg19UCSC Ensembl
Innerchr1:68984641..69095810hg18UCSC Ensembl
Innerchr1:68924074..69035243hg17UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg38111170
hg19111170
hg18111170
hg17111170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704203
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527722
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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