A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15195063



Internal ID21333966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24212556..24212556hg38UCSC Ensembl
chr14:24681762..24681762hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926645
Supporting Variants
SamplesHG002
Known GenesCHMP4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15195063
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