A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469738



Internal ID247514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36348839..36356759hg38UCSC Ensembl
chr4:36350461..36358381hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg387921
hg197921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469738
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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