A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13953885



Internal ID3280025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122028000..122030029hg38UCSC Ensembl
Innerchr10:122028013..122030017hg38UCSC Ensembl
Outerchr10:122027988..122030042hg38UCSC Ensembl
chr10:123787515..123789544hg19UCSC Ensembl
Innerchr10:123787528..123789532hg19UCSC Ensembl
Outerchr10:123787503..123789557hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382030
hg192030
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624764
Supporting Variants
SamplesHG02891
Known GenesTACC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13953885
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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