A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525046



Internal ID15452339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:99803435..99809861hg38UCSC Ensembl
Innerchr1:100268991..100275417hg19UCSC Ensembl
Innerchr1:100041579..100048005hg18UCSC Ensembl
Innerchr1:99981012..99987438hg17UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg386427
hg196427
hg186427
hg176427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701091
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525046
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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