A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9646n54



Internal ID22777541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21094753..21444589hg38UCSC Ensembl
chr5:21094862..21444698hg19UCSC Ensembl
chr5:21130619..21480455hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38349837
hg19349837
hg18349837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597439, nsv597436
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9646n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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