A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13963161



Internal ID373750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123982697..123984810hg38UCSC Ensembl
Innerchr10:123982697..123984810hg38UCSC Ensembl
Outerchr10:123982570..123984952hg38UCSC Ensembl
chr10:125742213..125744326hg19UCSC Ensembl
Innerchr10:125742213..125744326hg19UCSC Ensembl
Outerchr10:125742086..125744468hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382114
hg192114
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624803
Supporting Variants
SamplesHG00108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13963161
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