A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624722



Internal ID7011572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120103716..120107375hg38UCSC Ensembl
Innerchr10:120103716..120107375hg38UCSC Ensembl
Outerchr10:120103383..120107601hg38UCSC Ensembl
chr10:121863228..121866887hg19UCSC Ensembl
Innerchr10:121863228..121866887hg19UCSC Ensembl
Outerchr10:121862895..121867113hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg383660
hg193660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13948187
SamplesHG00253
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624722
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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