A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432030



Internal ID21089583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158789910..159175550hg38UCSC Ensembl
chr7:158582601..158968241hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38385641
hg19385641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7208n223
Supporting Variantsnssv18227668
Samples
Known GenesESYT2, LINC00689, VIPR2, WDR60
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432030
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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