A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527556



Internal ID18825837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18631932..18737101hg38UCSC Ensembl
Innerchr13:19206072..19311241hg19UCSC Ensembl
Innerchr13:18104072..18209241hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38105170
hg19105170
hg18105170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037534
Supporting Variants
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)nssv3527556
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