A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5398n54



Internal ID22773293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:948940..949747hg38UCSC Ensembl
chr17:852180..852987hg19UCSC Ensembl
chr17:798930..799737hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38808
hg19808
hg18808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574118, nsv574132, nsv574119, nsv574121, nsv574126, nsv574120, nsv574116, nsv574127, nsv574128, nsv574113
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5398n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss98
Observed Complex0
Frequencyn/a


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