A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960162



Internal ID40749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170949987..171146241hg38UCSC Ensembl
chr4:171871138..172067392hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38196255
hg19196255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456744
Supporting Variants
Samples
Known GenesLOC100506122
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960162
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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