A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5444n54



Internal ID22773339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10268563..10298798hg38UCSC Ensembl
chr17:10171880..10202115hg19UCSC Ensembl
chr17:10112605..10142840hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3830236
hg1930236
hg1830236
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574345, nsv574346
SamplesHGDP01244, HGDP01305
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5444n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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