A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704371



Internal ID128037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78970492..78970902hg38UCSC Ensembl
chr15:79262834..79263244hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527786
Supporting Variants
Samples
Known GenesRASGRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704371
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003139


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