A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13858618



Internal ID3860434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70436517..70438256hg38UCSC Ensembl
Innerchr10:70436519..70438254hg38UCSC Ensembl
Outerchr10:70436515..70438258hg38UCSC Ensembl
chr10:72196273..72198012hg19UCSC Ensembl
Innerchr10:72196275..72198010hg19UCSC Ensembl
Outerchr10:72196271..72198014hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381740
hg191740
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623765
Supporting Variants
SamplesHG01783
Known GenesNODAL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13858618
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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