A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989730



Internal ID20556770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32732273..32816725hg38UCSC Ensembl
chr11:32753819..32838271hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3884453
hg1984453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470928
Supporting Variants
Samples
Known GenesCCDC73
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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