A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035799



Internal ID19125018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18471488..18687960hg38UCSC Ensembl
Innerchr13:19045628..19262100hg19UCSC Ensembl
Innerchr13:17943628..18160100hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38216473
hg19216473
hg18216473
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1598n100
Supporting Variantsnssv3526419, nssv3712704, nssv3526421, nssv3526427, nssv3712701, nssv3526420, nssv3712702, nssv3526426, nssv3526423, nssv3526429, nssv3526422, nssv3526424, nssv3526428, nssv3712698, nssv3712700, nssv3712699, nssv3712703, nssv3526430, nssv3526425
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)nsv1035799
Frequency
Sample Size11257
Observed Gain18
Observed Loss1
Observed Complex0
Frequencyn/a


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