A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843421



Internal ID15790691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56212400..56279978hg38UCSC Ensembl
Innerchr15:56504598..56572176hg19UCSC Ensembl
Innerchr15:54291890..54359468hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3867579
hg1967579
hg1867579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569547
Supporting Variants
Samples
Known GenesRFX7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843421
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