A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477395



Internal ID21134948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97262881..97263735hg38UCSC Ensembl
chr13:97915135..97915989hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184354
Samples
Known GenesMBNL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477395
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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