A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020857



Internal ID19110075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39389580..39527169hg38UCSC Ensembl
Innerchr8:39247099..39384688hg19UCSC Ensembl
Innerchr8:39366256..39503845hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38137590
hg19137590
hg18137590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7175n100
Supporting Variantsnssv3756700
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)nsv1020857
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer