A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995075



Internal ID20562115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88710645..88761572hg38UCSC Ensembl
chr11:88443813..88494740hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3850928
hg1950928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464410
Supporting Variants
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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