A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653753



Internal ID21602058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101334388..101334388hg38UCSC Ensembl
chr13:101986739..101986739hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096034
SamplesHG00512
Known GenesNALCN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653753
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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