A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019739



Internal ID19108957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39429596..39529434hg38UCSC Ensembl
Innerchr8:39287115..39386953hg19UCSC Ensembl
Innerchr8:39406272..39506110hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3899839
hg1999839
hg1899839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7180n100
Supporting Variantsnssv3685973, nssv3685974, nssv3685972, nssv3685970, nssv3685971
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)nsv1019739
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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