A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025923



Internal ID19115140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:120081144..120096467hg38UCSC Ensembl
Innerchr8:121093383..121108706hg19UCSC Ensembl
Innerchr8:121162564..121177887hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3815324
hg1915324
hg1815324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691471
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025923
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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