A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455543



Internal ID21113096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86387401..86394400hg38UCSC Ensembl
chr10:88147158..88154157hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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