A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455198



Internal ID21112751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57221685..57230274hg38UCSC Ensembl
chr10:58981445..58990034hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg388590
hg198590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv753n223
Supporting Variantsnssv17982328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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