A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524281



Internal ID15451574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:80405146..80408360hg38UCSC Ensembl
Innerchr8:81317381..81320595hg19UCSC Ensembl
Innerchr8:81479936..81483150hg18UCSC Ensembl
Innerchr8:81479936..81483150hg17UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg383215
hg193215
hg183215
hg173215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700180
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524281
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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