A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624540



Internal ID7011393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110396631..110400127hg38UCSC Ensembl
Innerchr10:110396637..110400121hg38UCSC Ensembl
Outerchr10:110396625..110400133hg38UCSC Ensembl
chr10:112156389..112159885hg19UCSC Ensembl
Innerchr10:112156395..112159879hg19UCSC Ensembl
Outerchr10:112156383..112159891hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg383497
hg193497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13933965
SamplesNA19086
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624540
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