A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539713



Internal ID20913008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44531074..44531404hg38UCSC Ensembl
chr22:44926954..44927284hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074444
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539713
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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