A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798874



Internal ID16092830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:78388898..78427036hg38UCSC Ensembl
Innerchr12:78782678..78820816hg19UCSC Ensembl
Innerchr12:77306809..77344947hg18UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3838139
hg1938139
hg1838139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559437
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)nssv798874
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