A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189510



Internal ID20756550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76790215..76800173hg38UCSC Ensembl
chr17:74786297..74796255hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg389959
hg199959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189510
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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