A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623803



Internal ID7010659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72675476..72681322hg38UCSC Ensembl
Innerchr10:72675496..72681303hg38UCSC Ensembl
Outerchr10:72675457..72681342hg38UCSC Ensembl
chr10:74435234..74441080hg19UCSC Ensembl
Innerchr10:74435254..74441061hg19UCSC Ensembl
Outerchr10:74435215..74441100hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg385847
hg195847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861662, essv13861661
SamplesHG04029, HG03848
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623803
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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