A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5747n54



Internal ID22773642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65946135..66137608hg38UCSC Ensembl
chr17:63942253..64133726hg19UCSC Ensembl
chr17:61372715..61564188hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38191474
hg19191474
hg18191474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575877, nsv575880, nsv575881
Samples
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5747n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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