A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839282



Internal ID15786552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27158056..27164571hg38UCSC Ensembl
Innerchr15:27403203..27409718hg19UCSC Ensembl
Innerchr15:24985949..24992464hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg386516
hg196516
hg186516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568656
Supporting Variants
Samples
Known GenesGABRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839282
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