A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316908



Internal ID20849990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178402916..178420223hg38UCSC Ensembl
chr1:178372051..178389358hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3817308
hg1917308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201100
Samples
Known GenesRASAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316908
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