A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604000



Internal ID21552667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79840183..79840238hg38UCSC Ensembl
chr15:80132525..80132580hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091158
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604000
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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