A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633291



Internal ID7020100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97394950..97420813hg38UCSC Ensembl
Innerchr13:97394950..97420813hg38UCSC Ensembl
Outerchr13:97394450..97421313hg38UCSC Ensembl
chr13:98047204..98073067hg19UCSC Ensembl
Innerchr13:98047204..98073067hg19UCSC Ensembl
Outerchr13:98046704..98073567hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3825864
hg1925864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869393
SamplesHG04029
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633291
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