A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524762



Internal ID20898123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68160261..68192303hg38UCSC Ensembl
chr17:66156402..66188444hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3832043
hg1932043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182390
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524762
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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