A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703586



Internal ID127252
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 StatusS
Merged Variantsnsv5519128
Supporting Variants
Samples
Known GenesSEC11A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703586
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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