A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445939



Internal ID21103492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96741481..96863870hg38UCSC Ensembl
chr10:98501238..98623627hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38122390
hg19122390
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180360
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445939
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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