A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559231



Internal ID16346640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:69896210..69896905hg38UCSC Ensembl
Innerchr12:70289990..70290685hg19UCSC Ensembl
Innerchr12:68576257..68576952hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38696
hg19696
hg18696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2685n54
Supporting Variantsnssv797695, nssv797694
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559231
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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