A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033795



Internal ID19123016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:99545116..99654412hg38UCSC Ensembl
Innerchr8:100557344..100666640hg19UCSC Ensembl
Innerchr8:100626520..100735816hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38109297
hg19109297
hg18109297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689743
Samples
Known GenesVPS13B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033795
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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