A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187202



Internal ID20754242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50767900..50808786hg38UCSC Ensembl
chr17:48845261..48886147hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3840887
hg1940887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517841
Supporting Variants
Samples
Known GenesMIR8059
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187202
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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