A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416613



Internal ID21074166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133262308..133264575hg38UCSC Ensembl
chr7:132947063..132949330hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382268
hg192268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151580
Samples
Known GenesEXOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416613
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