A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035444



Internal ID19124663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38298550..38340379hg38UCSC Ensembl
Innerchr11:38320100..38361929hg19UCSC Ensembl
Innerchr11:38276676..38318505hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3841830
hg1941830
hg1841830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1102n100
Supporting Variantsnssv3710111
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035444
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