A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197011



Internal ID22346937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160507284..160659905hg38UCSC Ensembl
chr6:160928316..161080937hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38152622
hg19152622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330537, nssv14330536
SamplesNA19238, HG00514
Known GenesLPA, LPAL2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197011
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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