A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv558335



Internal ID16345744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:34635973..34701368hg38UCSC Ensembl
Innerchr12:34788908..34854303hg19UCSC Ensembl
Innerchr12:34680175..34745570hg18UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3865396
hg1965396
hg1865396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2520n54
Supporting Variantsnssv793117
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv558335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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