A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5394n54



Internal ID22773289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:947302..949686hg38UCSC Ensembl
chr17:850542..852926hg19UCSC Ensembl
chr17:797292..799676hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg382385
hg192385
hg182385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574102, nsv574103
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5394n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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