A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514690



Internal ID291184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71119386..71128246hg38UCSC Ensembl
chr15:71411725..71420585hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388861
hg198861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514690
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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