A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705541



Internal ID129207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96270214..96271586hg38UCSC Ensembl
chr15:96813443..96814815hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381373
hg191373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533604
Supporting Variants
Samples
Known GenesNR2F2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705541
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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