A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623848



Internal ID6664015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75223245..75223895hg38UCSC Ensembl
Innerchr10:75223246..75223894hg38UCSC Ensembl
Outerchr10:75223244..75223896hg38UCSC Ensembl
chr10:76983003..76983653hg19UCSC Ensembl
Innerchr10:76983004..76983652hg19UCSC Ensembl
Outerchr10:76983002..76983654hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863964, essv13863960, essv13863959, essv13863961, essv13863966, essv13863963, essv13863965, essv13863962
SamplesHG04229, HG03717, HG03950, HG03911, HG03594, HG03814, HG04225, HG03779
Known GenesVDAC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623848
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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