A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9135n54



Internal ID20142559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76040649..76053198hg38UCSC Ensembl
chr4:76961802..76974351hg19UCSC Ensembl
chr4:77180826..77193375hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3812550
hg1912550
hg1812550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594692, nsv594691
Samples
Known GenesART3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9135n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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