A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv788981



Internal ID15736251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:15927715..16010449hg38UCSC Ensembl
Innerchr12:16080649..16163383hg19UCSC Ensembl
Innerchr12:15971916..16054650hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3882735
hg1982735
hg1882735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557636
Supporting Variants
Samples
Known GenesDERA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv788981
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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