A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374617



Internal ID22600286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64041459..64081870hg38UCSC Ensembl
chr16:64075363..64115774hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3840412
hg1940412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374617
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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