A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609262



Internal ID20982333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75699796..75789475hg38UCSC Ensembl
chr7:75329114..75418793hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3889680
hg1989680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6911n223
Supporting Variantsnssv18226924
Samples
Known GenesCCL26, HIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609262
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