A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998761



Internal ID19189562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:185520454..185522933hg38UCSC Ensembl
Outerchr4:186441608..186444087hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382480
hg192480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149972
Supporting Variants
SamplesKWB1
Known GenesPDLIM3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998761
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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