A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377957



Internal ID22435827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65297063..65297063hg38UCSC Ensembl
chr16:65330966..65330966hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975032
Supporting Variants
Samples
Known GenesLINC00922
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377957
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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