A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537038



Internal ID20910377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61316683..61319836hg38UCSC Ensembl
chr20:59891739..59894892hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383154
hg193154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068284
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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