A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175895



Internal ID15854197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115209706..115234477hg38UCSC Ensembl
Innerchr12:115647511..115672282hg19UCSC Ensembl
Innerchr12:114131894..114156665hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3824772
hg1924772
hg1824772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560299
Supporting Variants
Samples1780862015_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175895
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