A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025935



Internal ID18768467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102186979..102456094hg38UCSC Ensembl
Innerchr8:103199207..103468322hg19UCSC Ensembl
Innerchr8:103268383..103537498hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38269116
hg19269116
hg18269116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691255
Samples
Known GenesRRM2B, UBR5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025935
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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