A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034700



Internal ID19123921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85831027..85888423hg38UCSC Ensembl
Innerchr8:86843256..86900652hg19UCSC Ensembl
Innerchr8:86912544..86969768hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3857397
hg1957397
hg1857225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7260n100
Supporting Variantsnssv3757313
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)nsv1034700
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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