A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988228



Internal ID20555268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134008728..134009046hg38UCSC Ensembl
chr11:133878623..133878941hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988228
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00164


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