A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360136



Internal ID22585805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75222150..75222321hg38UCSC Ensembl
chr11:74933195..74933366hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924298
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360136
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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