A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371595



Internal ID21029148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33018801..33025400hg38UCSC Ensembl
chr4:33020423..33027022hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115608
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371595
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