A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516065



Internal ID20889426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70409032..70419320hg38UCSC Ensembl
chr17:68405173..68415461hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3810289
hg1910289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516065
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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