A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549194



Internal ID20922362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64177312..64187823hg38UCSC Ensembl
chr20:62808665..62819176hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810512
hg1910512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070287
Samples
Known GenesMYT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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