A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998634



Internal ID18843123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:79558572..79558643hg38UCSC Ensembl
Outerchr4:80479726..80479797hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149846
Supporting Variants
SamplesKWB1
Known GenesLINC00989
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998634
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