A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13899289



Internal ID4276326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93196048..93197344hg38UCSC Ensembl
Innerchr10:93196098..93197294hg38UCSC Ensembl
Outerchr10:93195998..93197394hg38UCSC Ensembl
chr10:94955805..94957101hg19UCSC Ensembl
Innerchr10:94955855..94957051hg19UCSC Ensembl
Outerchr10:94955755..94957151hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381297
hg191297
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624235
Supporting Variants
SamplesHG03844
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13899289
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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