A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456744



Internal ID234805
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 StatusM
Merged Variants
Supporting Variantsnssv16960162
Samples
Known GenesLOC100506122
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456744
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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