A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993821



Internal ID20560861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63949522..63951985hg38UCSC Ensembl
chr11:63716994..63719457hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382464
hg192464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456543
Supporting Variants
Samples
Known GenesNAA40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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