A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373262



Internal ID22598931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12318668..12335797hg38UCSC Ensembl
chr16:12412525..12429654hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817130
hg1917130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930389
Supporting Variants
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373262
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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