A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357929



Internal ID22583598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27232400..27233448hg38UCSC Ensembl
chr11:27253947..27254995hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357929
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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