A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523655



Internal ID15450948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95193692..95226885hg38UCSC Ensembl
Innerchr8:96205920..96239113hg19UCSC Ensembl
Innerchr8:96275096..96308289hg18UCSC Ensembl
Innerchr8:96275096..96308289hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3833194
hg1933194
hg1833194
hg1733194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699456
Samples
Known GenesC8orf69
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523655
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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