A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382668



Internal ID22440538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2599918..2678342hg38UCSC Ensembl
chr16:2649919..2728343hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3878425
hg1978425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932235
Supporting Variants
Samples
Known GenesERVK13-1, FLJ42627, LOC652276, PDPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382668
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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