A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037233



Internal ID19126452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55294078..55404093hg38UCSC Ensembl
Innerchr13:55868213..55978228hg19UCSC Ensembl
Innerchr13:54766214..54876229hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38110016
hg19110016
hg18110016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1657n100
Supporting Variantsnssv3523865
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)nsv1037233
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