A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390141



Internal ID22448011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44990143..44990211hg38UCSC Ensembl
chr21:46410058..46410126hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950491
Supporting Variants
Samples
Known GenesLINC00163
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390141
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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