A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848136



Internal ID16142092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87249097..87334019hg38UCSC Ensembl
Innerchr15:87792328..87877250hg19UCSC Ensembl
Innerchr15:85593332..85678254hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3884923
hg1984923
hg1884923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570362
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv848136
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