A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646670



Internal ID21594975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61877438..61877438hg38UCSC Ensembl
chr15:62169637..62169637hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095485
SamplesHG00731
Known GenesVPS13C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646670
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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