A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024405



Internal ID19113622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124856442..124958793hg38UCSC Ensembl
Innerchr8:125868684..125971035hg19UCSC Ensembl
Innerchr8:125937865..126040216hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38102352
hg19102352
hg18102352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7310n100
Supporting Variantsnssv3691509
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)nsv1024405
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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