A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522767



Internal ID20896128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69563040..69564033hg38UCSC Ensembl
chr17:67559181..67560174hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037651
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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