A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13765119



Internal ID3766935
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623074
Supporting Variants
SamplesHG03913
Known GenesTMEM72-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13765119
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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