A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843332



Internal ID15790602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55240013..55318928hg38UCSC Ensembl
Innerchr15:55532211..55611126hg19UCSC Ensembl
Innerchr15:53319503..53398418hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3878916
hg1978916
hg1878916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569522
Supporting Variants
Samples
Known GenesRAB27A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843332
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