A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023401



Internal ID19112618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39429159..39522136hg38UCSC Ensembl
Innerchr8:39286678..39379655hg19UCSC Ensembl
Innerchr8:39405835..39498812hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3892978
hg1992978
hg1892978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7180n100
Supporting Variantsnssv3685962
Samples
Known GenesADAM3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023401
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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