A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380889



Internal ID21038442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163587832..163588357hg38UCSC Ensembl
chr4:164508984..164509509hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114390
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380889
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