A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148347



Internal ID15654847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136976551..136978985hg38UCSC Ensembl
Innerchr9:139871003..139873437hg19UCSC Ensembl
Innerchr9:138990824..138993258hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382435
hg192435
hg182435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615995
Supporting Variants
Samples
Known GenesPTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148347
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