A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032142



Internal ID18774676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28759983..28809934hg38UCSC Ensembl
Innerchr8:28617500..28667451hg19UCSC Ensembl
Innerchr8:28673419..28723370hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3849952
hg1949952
hg1849952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7159n100
Supporting Variantsnssv3685548
Samples
Known GenesINTS9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032142
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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