A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019380



Internal ID19108598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39440702..39529434hg38UCSC Ensembl
Innerchr8:39298221..39386953hg19UCSC Ensembl
Innerchr8:39417378..39506110hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3888733
hg1988733
hg1888733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7180n100
Supporting Variantsnssv3757164
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)nsv1019380
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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