A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038355



Internal ID21947698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87622910..87625991hg38UCSC Ensembl
chr13:88275165..88278246hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg383082
hg193082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609616
Samples
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038355
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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