A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486769



Internal ID22544684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61593838..61608976hg38UCSC Ensembl
chr20:60168894..60184032hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3815139
hg1915139
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872780
Supporting Variants
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486769
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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