A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602112



Internal ID21794159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2610455..2688315hg38UCSC Ensembl
chr16:2660456..2738316hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3877861
hg1977861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034892
Supporting Variants
Samples
Known GenesERVK13-1, FLJ42627, KCTD5, LOC652276
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602112
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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