A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523390



Internal ID20896751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72217695..72251435hg38UCSC Ensembl
chr17:70213836..70247576hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3833741
hg1933741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523390
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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