A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11539n54



Internal ID22779434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102232361..102305844hg38UCSC Ensembl
chr7:101875641..101949128hg19UCSC Ensembl
chr7:101662361..101735848hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3873484
hg1973488
hg1873488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607996, nsv607997
Samples
Known GenesCUX1, MIR4285, SH2B2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11539n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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