A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133623



Internal ID19279022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:133400..202100hg38UCSC Ensembl
Outerchr6:133400..202100hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3868701
hg1968701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3246n106
Supporting Variantsnssv3969187
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133623
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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