A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397018



Internal ID22454888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61593490..61631313hg38UCSC Ensembl
chr20:60168546..60206369hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3837824
hg1937824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954743
Supporting Variants
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397018
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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