A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891251



Internal ID168352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155874478..155875220hg38UCSC Ensembl
chr1:155844269..155845011hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418728
Supporting Variants
Samples
Known GenesSYT11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891251
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.030752


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