A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1458n54



Internal ID22769353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132345217..132477022hg38UCSC Ensembl
chr10:134158721..134290526hg19UCSC Ensembl
chr10:134008711..134140516hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38131806
hg19131806
hg18131806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552506, nsv552507
SamplesNINDS_60, NINDS_50
Known GenesC10orf91, LRRC27, PWWP2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1458n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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