A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551280



Internal ID20924417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26466756..26478291hg38UCSC Ensembl
chr22:26862722..26874257hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3811536
hg1911536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073168
Samples
Known GenesHPS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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