A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691256



Internal ID18989537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102356987..102526480hg38UCSC Ensembl
Innerchr8:103369215..103538708hg19UCSC Ensembl
Innerchr8:103438391..103607884hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38169494
hg19169494
hg18169494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023938
Supporting Variants
Samples
Known GenesUBR5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691256
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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