A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431042



Internal ID21088595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128728804..128731670hg38UCSC Ensembl
chr7:128368858..128371724hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg382867
hg192867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153322
Samples
Known GenesFAM71F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431042
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