A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604207



Internal ID20977278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87745129..87862781hg38UCSC Ensembl
chr7:87374445..87492096hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38117653
hg19117652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220849
Samples
Known GenesRUNDC3B, SLC25A40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604207
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