A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13685665



Internal ID2644147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5804504..5809863hg38UCSC Ensembl
Innerchr10:5804504..5809863hg38UCSC Ensembl
Outerchr10:5804369..5809996hg38UCSC Ensembl
chr10:5846467..5851826hg19UCSC Ensembl
Innerchr10:5846467..5851826hg19UCSC Ensembl
Outerchr10:5846332..5851959hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385360
hg195360
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622234
Supporting Variants
SamplesHG02337
Known GenesGDI2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13685665
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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