A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949102



Internal ID22724555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61387316..61387401hg38UCSC Ensembl
chr20:59962372..59962457hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409306
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949102
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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