A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746457



Internal ID21393030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157309969..157314968hg38UCSC Ensembl
chr6:157731001..157736000hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434798
Supporting Variants
SamplesSMI041
Known GenesTMEM242
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746457
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