A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14312558



Internal ID22315473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24964831..24965505hg38UCSC Ensembl
chr4:24966453..24967127hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526524
Supporting Variants
SamplesNA19240
Known GenesCCDC149
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14312558
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