A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653357



Internal ID21601662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7071557..7071557hg38UCSC Ensembl
chr11:7092788..7092788hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076147
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653357
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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