A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354391



Internal ID22580060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61041382..61046522hg38UCSC Ensembl
chr11:60808854..60813994hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg385141
hg195141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354391
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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