A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798870



Internal ID16092826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:77446162..77511427hg38UCSC Ensembl
Innerchr12:77839942..77905207hg19UCSC Ensembl
Innerchr12:76364073..76429338hg18UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3865266
hg1965266
hg1865266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559428
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)nssv798870
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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