A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9265n54



Internal ID22777160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:130605780..130708805hg38UCSC Ensembl
chr4:131526935..131629960hg19UCSC Ensembl
chr4:131746385..131849410hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38103026
hg19103026
hg18103026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595420, nsv595419
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9265n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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