A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519890



Internal ID20893251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54079901..54090500hg38UCSC Ensembl
chr17:52157262..52167861hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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