A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020502



Internal ID19109721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124856442..124960330hg38UCSC Ensembl
Innerchr8:125868684..125972572hg19UCSC Ensembl
Innerchr8:125937865..126041753hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38103889
hg19103889
hg18103889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7310n100
Supporting Variantsnssv3691510
Samples
Known GenesLINC00964
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020502
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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