A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083033



Internal ID21283391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156909717..156919879hg38UCSC Ensembl
Innerchr6:157230851..157241013hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3810163
hg1910163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117011
Supporting Variants
Samplessample343
Known GenesARID1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083033
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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