A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955662



Internal ID22730863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61714172..61741755hg38UCSC Ensembl
chr20:60289228..60316811hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3827584
hg1927584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1330n209
Supporting Variantsnssv17402163
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955662
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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