A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234543



Internal ID20801583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32121063..32179177hg38UCSC Ensembl
chr7:32160675..32218789hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3858115
hg1958115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602956
Supporting Variants
Samples
Known GenesPDE1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234543
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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