A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449398



Internal ID227634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15174700..15279400hg38UCSC Ensembl
chr4:15176324..15281024hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38104701
hg19104701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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