A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518899



Internal ID295262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96296005..96296345hg38UCSC Ensembl
chr15:96839234..96839574hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705542
Samples
Known GenesNR2F2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518899
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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