A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189753



Internal ID20756793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76810090..76834140hg38UCSC Ensembl
chr17:74806172..74830222hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3824051
hg1924051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189753
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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