A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661545



Internal ID21609850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34540984..34540984hg38UCSC Ensembl
chr13:35115121..35115121hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095707
SamplesHG00731
Known GenesLINC00457
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661545
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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