A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443693



Internal ID21101246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97406795..97408429hg38UCSC Ensembl
chr10:99166552..99168186hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381635
hg191635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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