A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5756n54



Internal ID22773651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68102769..68187221hg38UCSC Ensembl
chr17:66098910..66183362hg19UCSC Ensembl
chr17:63610547..63694957hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3884453
hg1984453
hg1884411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575925, nsv575923, nsv575924, nsv575926
Samples
Known GenesLINC00674
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5756n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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