A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953684



Internal ID22728963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61674526..61676889hg38UCSC Ensembl
chr20:60249582..60251945hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382364
hg192364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390046
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953684
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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