A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154032



Internal ID19200851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:29229509..29229842hg38UCSC Ensembl
Outerchr21:30601830..30602163hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003304
SamplesKWB1
Known GenesLINC00189
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1154032
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