A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11222n54



Internal ID20144646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16133267..16134327hg38UCSC Ensembl
chr7:16172892..16173952hg19UCSC Ensembl
chr7:16139417..16140477hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381061
hg191061
hg181061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606320, nsv606322
Samples
Known GenesISPD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11222n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss121
Observed Complex0
Frequencyn/a


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