A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037573



Internal ID19126792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120359534..120416209hg38UCSC Ensembl
Innerchr11:120230243..120286918hg19UCSC Ensembl
Innerchr11:119735453..119792128hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3856676
hg1956676
hg1856676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1287n100
Supporting Variantsnssv3505113
Samples
Known GenesARHGEF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037573
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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