A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450364



Internal ID21107917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45450031..45452856hg38UCSC Ensembl
chr10:45945479..45948304hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382826
hg192826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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