A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703183



Internal ID126849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60869679..60871339hg38UCSC Ensembl
chr15:61161878..61163538hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381661
hg191661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518276
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703183
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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