A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151983



Internal ID19201791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:152599569..152599707hg38UCSC Ensembl
Outerchr3:152317358..152317496hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999162
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151983
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