A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645788



Internal ID21594093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100615041..100615041hg38UCSC Ensembl
chr13:101267295..101267295hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089666
SamplesNA19650
Known GenesTMTC4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645788
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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