A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950251



Internal ID22725657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61692678..61722291hg38UCSC Ensembl
chr20:60267734..60297347hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3829614
hg1929614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409630
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950251
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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