A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615492



Internal ID21563797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1173729..1173729hg38UCSC Ensembl
chr7:63602261..63602261hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169548
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615492
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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