A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988055



Internal ID20555095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132736683..132737313hg38UCSC Ensembl
chr11:132606578..132607208hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475279
Supporting Variants
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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