A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525564



Internal ID18823845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105499401..105539918hg38UCSC Ensembl
Innerchr13:106151750..106192267hg19UCSC Ensembl
Innerchr13:104949751..104990268hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3840518
hg1940518
hg1840518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052425
Supporting Variants
Samples
Known GenesDAOA-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525564
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