A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705157



Internal ID15441809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142825472..142838881hg38UCSC Ensembl
Innerchr8:143906888..143920297hg19UCSC Ensembl
Innerchr8:143903890..143917299hg18UCSC Ensembl
Innerchr8:143903890..143917299hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3813410
hg1913410
hg1813410
hg1713410
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528545
Supporting Variants
Samples
Known GenesGML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705157
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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