A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623060



Internal ID7009917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44261796..44265806hg38UCSC Ensembl
Innerchr10:44261796..44265806hg38UCSC Ensembl
Outerchr10:44261624..44266031hg38UCSC Ensembl
chr10:44757244..44761254hg19UCSC Ensembl
Innerchr10:44757244..44761254hg19UCSC Ensembl
Outerchr10:44757072..44761479hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384011
hg194011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764988, essv13764989, essv13764987
SamplesHG00143, NA12750, NA11918
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623060
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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