A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619112



Internal ID20992183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14975901..14996400hg38UCSC Ensembl
chr7:15015526..15036025hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3820500
hg1920500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6594n223
Supporting Variantsnssv18235034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619112
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