A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993155



Internal ID20560195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61663717..61665099hg38UCSC Ensembl
chr11:61431189..61432571hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381383
hg191383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00035


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