A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994079



Internal ID20561119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64992148..64994936hg38UCSC Ensembl
chr11:64759620..64762408hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382789
hg192789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468325
Supporting Variants
Samples
Known GenesBATF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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