A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545113



Internal ID15985836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3167623..3167778hg38UCSC Ensembl
Innerchr1:3084187..3084342hg19UCSC Ensembl
Innerchr1:3074047..3074202hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38156
hg19156
hg18156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708801
Samples
Known GenesPRDM16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545113
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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