A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472737



Internal ID250441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40377005..40384115hg38UCSC Ensembl
chr4:40379022..40386132hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg387111
hg197111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948123
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472737
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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