A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699719



Internal ID123385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30084200..30590437hg38UCSC Ensembl
chr15:30376403..30882640hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38506238
hg19506238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505864
Supporting Variants
Samples
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699719
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008959


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