A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073803



Internal ID20640843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39997541..40001275hg38UCSC Ensembl
chr22:40393545..40397279hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383735
hg193735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540105
Supporting Variants
Samples
Known GenesFAM83F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001


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