A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623921



Internal ID6664088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79687526..79795112hg38UCSC Ensembl
Innerchr10:79688026..79794612hg38UCSC Ensembl
Outerchr10:79686526..79796112hg38UCSC Ensembl
chr10:81447282..81554868hg19UCSC Ensembl
Innerchr10:81447782..81554368hg19UCSC Ensembl
Outerchr10:81446282..81555868hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38107587
hg19107587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13868345, essv13868341, essv13868340, essv13868338, essv13868344, essv13868342, essv13868343, essv13868339, essv13868337
SamplesHG02275, HG02006, NA19795, HG02277, NA19654, NA11994, HG02017, HG02271, HG01892
Known GenesBEND3P3, NUTM2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623921
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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