A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035344



Internal ID19124563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104763258..104795567hg38UCSC Ensembl
Innerchr13:105415609..105447918hg19UCSC Ensembl
Innerchr13:104213610..104245919hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3832310
hg1932310
hg1832310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1737n100
Supporting Variantsnssv3525551
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)nsv1035344
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