A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612703



Internal ID20985774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24755801..24760800hg38UCSC Ensembl
chr7:24795420..24800419hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219323
Samples
Known GenesDFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612703
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