A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526171



Internal ID15453464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96349606..96483768hg38UCSC Ensembl
Innerchr8:97361834..97495996hg19UCSC Ensembl
Innerchr8:97431010..97565172hg18UCSC Ensembl
Innerchr8:97431010..97565172hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38134163
hg19134163
hg18134163
hg17134163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702432
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526171
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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