A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383831



Internal ID22441701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6345004..6653510hg38UCSC Ensembl
chr16:6395005..6703511hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38308507
hg19308507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932172
Supporting Variants
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383831
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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