A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624688



Internal ID7011538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118346150..118347682hg38UCSC Ensembl
Innerchr10:118346200..118347632hg38UCSC Ensembl
Outerchr10:118346100..118347732hg38UCSC Ensembl
chr10:120105662..120107194hg19UCSC Ensembl
Innerchr10:120105712..120107144hg19UCSC Ensembl
Outerchr10:120105612..120107244hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381533
hg191533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946602, essv13946603
SamplesNA18547, NA19075
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624688
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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