A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545456



Internal ID20918687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41898346..41898964hg38UCSC Ensembl
chr21:43318455..43319073hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071561
Samples
Known GenesC2CD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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