A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994601



Internal ID20561641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8619927..8620716hg38UCSC Ensembl
chr11:8641474..8642263hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441354
Supporting Variants
Samples
Known GenesTRIM66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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