A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623074



Internal ID6663242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44856021..44861644hg38UCSC Ensembl
Innerchr10:44856071..44861594hg38UCSC Ensembl
Outerchr10:44855831..44861834hg38UCSC Ensembl
chr10:45351469..45357092hg19UCSC Ensembl
Innerchr10:45351519..45357042hg19UCSC Ensembl
Outerchr10:45351279..45357282hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385624
hg195624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13765118, essv13765122, essv13765121, essv13765119, essv13765123, essv13765120
SamplesNA20903, HG03598, HG03941, NA21099, HG04162, HG03913
Known GenesTMEM72-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623074
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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