A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9884n54



Internal ID20143308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76528140..76618904hg38UCSC Ensembl
chr5:75823965..75914729hg19UCSC Ensembl
chr5:75859721..75950485hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3890765
hg1990765
hg1890765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598680, nsv598679
Samples
Known GenesF2RL2, IQGAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9884n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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