A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364948



Internal ID21022501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27416117..27556466hg38UCSC Ensembl
chr3:27457608..27597957hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38140350
hg19140350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210466
Samples
Known GenesSLC4A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364948
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