A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5610n54



Internal ID20139034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45509805..45519155hg38UCSC Ensembl
chr17:43587171..43596521hg19UCSC Ensembl
chr17:40942954..40952304hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg389351
hg199351
hg189351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575104, nsv575105
Samples
Known GenesLRRC37A4P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5610n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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