A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538780



Internal ID20912094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61542349..61672570hg38UCSC Ensembl
chr20:60117405..60247626hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38130222
hg19130222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068299
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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