A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190258



Internal ID20757298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76325161..76347238hg38UCSC Ensembl
chr17:74321242..74343319hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3822078
hg1922078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517561
Supporting Variants
Samples
Known GenesPRPSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190258
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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