A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731660



Internal ID20507580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13741855..13747159hg38UCSC Ensembl
chr16:13835712..13841016hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385305
hg195305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275314
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731660
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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