A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999619



Internal ID67326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91171156..91171295hg38UCSC Ensembl
chr7:90800471..90800610hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492191
Supporting Variants
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999619
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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