A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545443



Internal ID20918674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59905001..59906900hg38UCSC Ensembl
chr20:58480056..58481955hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069178
Samples
Known GenesSYCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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