A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624804



Internal ID7011654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124267163..124270758hg38UCSC Ensembl
Innerchr10:124267165..124270757hg38UCSC Ensembl
Outerchr10:124267162..124270760hg38UCSC Ensembl
chr10:125955732..125959327hg19UCSC Ensembl
Innerchr10:125955734..125959326hg19UCSC Ensembl
Outerchr10:125955731..125959329hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383596
hg193596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171e214
Supporting Variantsessv13963164, essv13963165, essv13963167, essv13963166
SamplesHG01441, HG00306, HG01369, HG01378
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624804
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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