A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526716



Internal ID20900077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72387282..72398520hg38UCSC Ensembl
chr17:70383423..70394661hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3811239
hg1911239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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