A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519128



Internal ID295484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84688551..84690288hg38UCSC Ensembl
chr15:85231782..85233519hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381738
hg191738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703586
Samples
Known GenesSEC11A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519128
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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