A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018802



Internal ID18761335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38170677..38248634hg38UCSC Ensembl
Innerchr8:38028195..38106152hg19UCSC Ensembl
Innerchr8:38147352..38225309hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3877958
hg1977958
hg1877958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7162n100
Supporting Variantsnssv3685571
Samples
Known GenesBAG4, DDHD2, LSM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018802
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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