A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202775



Internal ID21341579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52672314..52672314hg38UCSC Ensembl
chr6:52537112..52537112hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928131
Supporting Variants
SamplesHG002
Known GenesTMEM14A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202775
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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