A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221554



Internal ID20788594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65035202..65870265hg38UCSC Ensembl
chr7:64495580..65335252hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38835064
hg19839673
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619355
Supporting Variants
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00019


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