A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624566



Internal ID7011419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111649781..111652763hg38UCSC Ensembl
Innerchr10:111649797..111652747hg38UCSC Ensembl
Outerchr10:111649765..111652779hg38UCSC Ensembl
chr10:113409539..113412521hg19UCSC Ensembl
Innerchr10:113409555..113412505hg19UCSC Ensembl
Outerchr10:113409523..113412537hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382983
hg192983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13935653, essv13935651, essv13935657, essv13935655, essv13935656, essv13935660, essv13935654, essv13935661, essv13935659, essv13935658, essv13935652
SamplesHG03297, NA19923, NA18874, NA18867, NA18934, HG02108, HG02594, HG02484, NA20289, NA18873, NA18876
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624566
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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