A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521991



Internal ID20895352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64664699..64667149hg38UCSC Ensembl
chr17:62660817..62663267hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg382451
hg192451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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