A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027074



Internal ID18769606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39368209..39527663hg38UCSC Ensembl
Innerchr8:39225728..39385182hg19UCSC Ensembl
Innerchr8:39344885..39504339hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38159455
hg19159455
hg18159455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3685612, nssv3685613, nssv3685611, nssv3685614
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)nsv1027074
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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