A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194554



Internal ID22344858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:93419091..93421013hg38UCSC Ensembl
chr4:94340242..94342164hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg381923
hg191923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314635, nssv14314634, nssv14314633
SamplesHG00731, HG00732, HG00733
Known GenesGRID2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194554
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