A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025103



Internal ID18767635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39372652..39539496hg38UCSC Ensembl
Innerchr8:39230171..39397015hg19UCSC Ensembl
Innerchr8:39349328..39516172hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38166845
hg19166845
hg18166845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3684961, nssv3683852, nssv3684966, nssv3684960, nssv3684965, nssv3684964, nssv3684963, nssv3684962
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025103
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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