A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926638



Internal ID22701865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96845764..96862809hg38UCSC Ensembl
chr10:98605521..98622566hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3817046
hg1917046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352465
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926638
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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