A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229075



Internal ID20796115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143387343..143388044hg38UCSC Ensembl
chr7:143084436..143085137hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431050
Supporting Variants
Samples
Known GenesZYX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229075
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer