A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073677



Internal ID20640717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30411563..30412578hg38UCSC Ensembl
chr22:30807552..30808567hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542890
Supporting Variants
Samples
Known GenesSEC14L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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