A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436397



Internal ID215014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71828973..71829726hg38UCSC Ensembl
chr3:71878124..71878877hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436397
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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