A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151674



Internal ID19202960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:131331455..131336356hg38UCSC Ensembl
Outerchr3:131050299..131055200hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg384902
hg194902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003097
SamplesKWB1
Known GenesLOC339874, NEK11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151674
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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