A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624685



Internal ID7011535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118280524..118283807hg38UCSC Ensembl
Innerchr10:118280535..118283797hg38UCSC Ensembl
Outerchr10:118280514..118283818hg38UCSC Ensembl
chr10:120040036..120043319hg19UCSC Ensembl
Innerchr10:120040047..120043309hg19UCSC Ensembl
Outerchr10:120040026..120043330hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383284
hg193284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946597, essv13946598, essv13946599
SamplesHG03817, HG03746, HG03785
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624685
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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