A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14325598



Internal ID22281857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36500697..36501010hg38UCSC Ensembl
chr6:36468474..36468787hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529731
Supporting Variants
SamplesNA19239
Known GenesSTK38
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14325598
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