A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658931



Internal ID21607236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75752772..75752772hg38UCSC Ensembl
chr13:76326908..76326908hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088120
SamplesHG00864
Known GenesLMO7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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