A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513767



Internal ID20887114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44128262..44136336hg38UCSC Ensembl
chr17:42205630..42213704hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg388075
hg198075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513767
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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