A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14315432



Internal ID22123691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99589070..99589166hg38UCSC Ensembl
chr4:100510227..100510323hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207393
Supporting Variants
SamplesHG00512
Known GenesMTTP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14315432
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