A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522526



Internal ID20895887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47189912..47192006hg38UCSC Ensembl
chr17:45267278..45269372hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg382095
hg192095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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