A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612382



Internal ID20985453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6854901..7029200hg38UCSC Ensembl
chr7:6894532..7068831hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38174300
hg19174300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6558n223
Supporting Variantsnssv18219595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612382
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