A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187668



Internal ID20754708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38796029..38807243hg38UCSC Ensembl
chr17:36952282..36963496hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3811215
hg1911215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501382
Supporting Variants
Samples
Known GenesCWC25, PIP4K2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187668
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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