A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622907



Internal ID7009765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35874576..35875831hg38UCSC Ensembl
Innerchr10:35874595..35875812hg38UCSC Ensembl
Outerchr10:35874557..35875850hg38UCSC Ensembl
chr10:36163504..36164759hg19UCSC Ensembl
Innerchr10:36163523..36164740hg19UCSC Ensembl
Outerchr10:36163485..36164778hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381256
hg191256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13753905
SamplesHG02082
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622907
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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