A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649901



Internal ID21598206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71768926..71768926hg38UCSC Ensembl
chr15:72061265..72061265hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089078
SamplesNA19238
Known GenesTHSD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649901
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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