A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528599



Internal ID15455892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69323238..69325689hg38UCSC Ensembl
Innerchr8:70235473..70237924hg19UCSC Ensembl
Innerchr8:70398027..70400478hg18UCSC Ensembl
Innerchr8:70398027..70400478hg17UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg382452
hg192452
hg182452
hg172452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705225
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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