A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522488



Internal ID15449781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97345154..97347784hg38UCSC Ensembl
Innerchr8:98357382..98360012hg19UCSC Ensembl
Innerchr8:98426558..98429188hg18UCSC Ensembl
Innerchr8:98426558..98429188hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382631
hg192631
hg182631
hg172631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705855
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522488
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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