A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1400n54



Internal ID22769295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115464095..115571554hg38UCSC Ensembl
chr10:117223605..117331064hg19UCSC Ensembl
chr10:117213595..117321054hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38107460
hg19107460
hg18107460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552205, nsv552207, nsv552204, nsv552206
Samples
Known GenesATRNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1400n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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