A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362663



Internal ID21020216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25524901..25526700hg38UCSC Ensembl
chr4:25526523..25528322hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362663
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