A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024283



Internal ID19113500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:135656274..135713488hg38UCSC Ensembl
Innerchr8:136668517..136725731hg19UCSC Ensembl
Innerchr8:136737699..136794913hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3857215
hg1957215
hg1857215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692721
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)nsv1024283
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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