A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5519n54



Internal ID22773414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30860479..30886925hg38UCSC Ensembl
chr17:29187497..29213943hg19UCSC Ensembl
chr17:26211623..26238069hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3826447
hg1926447
hg1826447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574665, nsv574666
Samples
Known GenesATAD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5519n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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