A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515879



Internal ID20889240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64286198..64292453hg38UCSC Ensembl
chr17:62363558..62369813hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg386256
hg196256
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515879
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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