A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610311



Internal ID21802358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78970484..78970922hg38UCSC Ensembl
chr15:79262826..79263264hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022590
Supporting Variants
Samples
Known GenesRASGRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610311
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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