A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891266



Internal ID168360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156059786..156061811hg38UCSC Ensembl
chr1:156029577..156031602hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg382026
hg192026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422141
Supporting Variants
Samples
Known GenesMIR7851, RAB25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891266
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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