A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13884019



Internal ID6188746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86683658..86684043hg38UCSC Ensembl
Innerchr10:86683689..86684012hg38UCSC Ensembl
Outerchr10:86683627..86684074hg38UCSC Ensembl
chr10:88443415..88443800hg19UCSC Ensembl
Innerchr10:88443446..88443769hg19UCSC Ensembl
Outerchr10:88443384..88443831hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624098
Supporting Variants
SamplesNA19720
Known GenesLDB3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13884019
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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