A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151175



Internal ID19197365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:113532997..113536898hg38UCSC Ensembl
Outerchr6:113854199..113858100hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002108
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151175
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