A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991955



Internal ID20558995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58736337..58836028hg38UCSC Ensembl
chr11:58503810..58603501hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3899692
hg1999692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468761
Supporting Variants
Samples
Known GenesGLYATL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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