A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523480



Internal ID15450773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25132941..25134157hg38UCSC Ensembl
Innerchr1:25459432..25460648hg19UCSC Ensembl
Innerchr1:25332019..25333235hg18UCSC Ensembl
Innerchr1:25204738..25205954hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381217
hg191217
hg181217
hg171217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699245
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523480
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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