A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624309



Internal ID6664476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97075279..97077338hg38UCSC Ensembl
Innerchr10:97075279..97077338hg38UCSC Ensembl
Outerchr10:97075002..97077638hg38UCSC Ensembl
chr10:98835036..98837095hg19UCSC Ensembl
Innerchr10:98835036..98837095hg19UCSC Ensembl
Outerchr10:98834759..98837395hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382060
hg192060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13905689, essv13905688
SamplesHG02032, HG01870
Known GenesSLIT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624309
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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