A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624758



Internal ID6664919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121712065..121717016hg38UCSC Ensembl
Innerchr10:121712106..121716975hg38UCSC Ensembl
Outerchr10:121712024..121717057hg38UCSC Ensembl
chr10:123471579..123476530hg19UCSC Ensembl
Innerchr10:123471620..123476489hg19UCSC Ensembl
Outerchr10:123471538..123476571hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384952
hg194952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13953794
SamplesHG03611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624758
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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