A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3557828



Internal ID22426632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58562830..58569373hg38UCSC Ensembl
chr4:59428995..59435538hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg386544
hg196544
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14313684, nssv14313685
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3557828
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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