A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455506



Internal ID21113059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23351617..23365994hg38UCSC Ensembl
chr10:23640546..23654923hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3814378
hg1914378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979723
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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