A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192612



Internal ID20759652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35757407..35761855hg38UCSC Ensembl
chr17:34084426..34088874hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384449
hg194449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498234
Supporting Variants
Samples
Known GenesC17orf50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192612
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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