A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891269



Internal ID168362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156152562..156152693hg38UCSC Ensembl
chr1:156122353..156122484hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421374
Supporting Variants
Samples
Known GenesMIR7851, SEMA4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891269
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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