A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14432670



Internal ID22175552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239068843..239069481hg38UCSC Ensembl
chr2:239990539..239991177hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3282844
Supporting Variants
SamplesHG00514
Known GenesHDAC4, MIR4440
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14432670
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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