A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526643



Internal ID22396025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138537921..138538307hg38UCSC Ensembl
chr5:137873610..137873996hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325736
SamplesNA19239
Known GenesETF1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526643
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