A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993238



Internal ID20560278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62864657..62871366hg38UCSC Ensembl
chr11:62632129..62638838hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg386710
hg196710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464618
Supporting Variants
Samples
Known GenesSLC3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993238
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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