A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391797



Internal ID21049350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:115000479..115001225hg38UCSC Ensembl
chr4:115921635..115922381hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106459
Samples
Known GenesNDST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391797
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