A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525287



Internal ID22394663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168704195..168704341hg38UCSC Ensembl
chr5:168131200..168131346hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14323757, nssv14323756, nssv14323755
SamplesNA19238, NA19239, NA19240
Known GenesSLIT3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525287
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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