A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746207



Internal ID21389631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157308969..157315968hg38UCSC Ensembl
chr6:157730001..157737000hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434797
Supporting Variants
SamplesNB09
Known GenesTMEM242
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746207
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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