A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585769



Internal ID347348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105478934..105480370hg38UCSC Ensembl
Outerchr13:105478789..105480809hg38UCSC Ensembl
Innerchr13:106131283..106132719hg19UCSC Ensembl
Outerchr13:106131138..106133158hg19UCSC Ensembl
Innerchr13:104929284..104930720hg18UCSC Ensembl
Outerchr13:104929139..104931159hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg382021
hg192021
hg182021
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275034
Supporting Variants
Samples
Known GenesDAOA, DAOA-AS1
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585769
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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