A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011573



Internal ID19100790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31860029..32251734hg38UCSC Ensembl
Innerchr3:31901521..32293226hg19UCSC Ensembl
Innerchr3:31876525..32268230hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38391706
hg19391706
hg18391706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589583
Samples
Known GenesCMTM8, GPD1L, OSBPL10, ZNF860
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011573
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