A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451784



Internal ID21109337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43432676..43449681hg38UCSC Ensembl
chr10:43928124..43945129hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3817006
hg1917006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981644
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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