A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540212



Internal ID20913504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42737544..42742520hg38UCSC Ensembl
chr21:44157654..44162630hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384977
hg194977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072507
Samples
Known GenesPDE9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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