A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513308



Internal ID20886651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34194236..34246414hg38UCSC Ensembl
chr17:32521255..32573433hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3852179
hg1952179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513308
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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