A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623769



Internal ID6663936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70839159..70843001hg38UCSC Ensembl
Innerchr10:70839159..70843001hg38UCSC Ensembl
Outerchr10:70839080..70843135hg38UCSC Ensembl
chr10:72598916..72602758hg19UCSC Ensembl
Innerchr10:72598916..72602758hg19UCSC Ensembl
Outerchr10:72598837..72602892hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383843
hg193843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13859160, essv13859159, essv13859161
SamplesHG01492, NA12778, HG00105
Known GenesSGPL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623769
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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