A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987860



Internal ID20554900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1250901..1251400hg38UCSC Ensembl
chr11:1272131..1272630hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452065
Supporting Variants
Samples
Known GenesMUC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01906


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