A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552056



Internal ID20925186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47331287..47477356hg38UCSC Ensembl
chr22:47727037..47873105hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38146070
hg19146069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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