A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091738



Internal ID21455953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74110645..74110783hg38UCSC Ensembl
chr15:74402986..74403124hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590781
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091738
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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