A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377286



Internal ID22435156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71839879..71840014hg38UCSC Ensembl
chr16:71873782..71873917hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377286
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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