A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551323



Internal ID20924460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38831650..38835646hg38UCSC Ensembl
chr22:39227655..39231651hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383997
hg193997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073998
Samples
Known GenesNPTXR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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