A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16894699



Internal ID170636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201961311..201961868hg38UCSC Ensembl
chr1:201930439..201930996hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446503
Supporting Variants
Samples
Known GenesTIMM17A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16894699
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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