A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993167



Internal ID20560207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62009215..62011533hg38UCSC Ensembl
chr11:61776687..61779005hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382319
hg192319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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