A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391680



Internal ID21049233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118841174..118845030hg38UCSC Ensembl
chr4:119762329..119766185hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383857
hg193857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108349
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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