A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13887863



Internal ID3889679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87858507..87860055hg38UCSC Ensembl
Innerchr10:87858517..87860046hg38UCSC Ensembl
Outerchr10:87858498..87860065hg38UCSC Ensembl
chr10:89618264..89619812hg19UCSC Ensembl
Innerchr10:89618274..89619803hg19UCSC Ensembl
Outerchr10:89618255..89619822hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381549
hg191549
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624115
Supporting Variants
SamplesNA19711
Known GenesKLLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13887863
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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