A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631765



Internal ID7018574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35430360..35467605hg38UCSC Ensembl
Innerchr13:35430860..35467105hg38UCSC Ensembl
Outerchr13:35429360..35468605hg38UCSC Ensembl
chr13:36004497..36041742hg19UCSC Ensembl
Innerchr13:36004997..36041242hg19UCSC Ensembl
Outerchr13:36003497..36042742hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3837246
hg1937246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14688581
SamplesHG00407
Known GenesNBEA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631765
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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