A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16894661



Internal ID170612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201410185..201422146hg38UCSC Ensembl
chr1:201379313..201391274hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3811962
hg1911962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442557
Supporting Variants
Samples
Known GenesTNNI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16894661
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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