A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519419



Internal ID20892780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73718789..73732410hg38UCSC Ensembl
chr17:71714928..71728549hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3813622
hg1913622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519419
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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