A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500110



Internal ID20873335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43667368..43719064hg38UCSC Ensembl
chr17:41744736..41796432hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3851697
hg1951697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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