A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2361n54



Internal ID20135785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10449091..10545656hg38UCSC Ensembl
chr12:10601690..10698255hg19UCSC Ensembl
chr12:10492957..10589522hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3896566
hg1996566
hg1896566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv557478, nsv557477
Samples
Known GenesKLRC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2361n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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