A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611310



Internal ID21559615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8239258..8239258hg38UCSC Ensembl
chr4:8240985..8240985hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124721
SamplesNA19239
Known GenesSH3TC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611310
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer