A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184896



Internal ID20751936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30621541..30866516hg38UCSC Ensembl
chr10:30910470..31155445hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38244976
hg19244976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444594
Supporting Variants
Samples
Known GenesLYZL2, SVILP1, ZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184896
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