A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13930279



Internal ID4076851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107363158..107367165hg38UCSC Ensembl
Innerchr10:107363163..107367160hg38UCSC Ensembl
Outerchr10:107363153..107367170hg38UCSC Ensembl
chr10:109122916..109126923hg19UCSC Ensembl
Innerchr10:109122921..109126918hg19UCSC Ensembl
Outerchr10:109122911..109126928hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg384008
hg194008
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624485
Supporting Variants
SamplesHG03708
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13930279
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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