A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097501



Internal ID21269127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:107000823..107085731hg38UCSC Ensembl
Innerchr5:106336524..106421432hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3884909
hg1984909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114198
Supporting Variants
Samplessample135
Known GenesLOC102467213
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097501
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