A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451782



Internal ID21109335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62665795..62666599hg38UCSC Ensembl
chr10:64425555..64426359hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982798
Samples
Known GenesZNF365
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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