A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187751



Internal ID20754791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67313254..67323889hg38UCSC Ensembl
chr17:65309370..65320005hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3810636
hg1910636
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187751
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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