A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464472



Internal ID242349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177045909..177229537hg38UCSC Ensembl
chr4:177967063..178150691hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38183629
hg19183629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961072
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464472
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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