A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441357



Internal ID21098910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43905466..43910676hg38UCSC Ensembl
chr10:44400914..44406124hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385211
hg195211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980306
Samples
Known GenesLINC00841
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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