A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624115



Internal ID6664282
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13887858, essv13887861, essv13887854, essv13887852, essv13887864, essv13887853, essv13887856, essv13887862, essv13887863, essv13887860, essv13887857, essv13887859, essv13887855
SamplesHG02337, NA18486, HG02323, NA20294, HG02054, NA18868, NA19238, NA19236, HG03124, HG02635, HG03458, NA19711, NA19312
Known GenesKLLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624115
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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