A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519207



Internal ID20892568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72239213..72253451hg38UCSC Ensembl
chr17:70235354..70249592hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3814239
hg1914239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519207
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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