A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1035n54



Internal ID20134459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35631696..35644550hg38UCSC Ensembl
chr10:35920624..35933478hg19UCSC Ensembl
chr10:35960630..35973484hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3812855
hg1912855
hg1812855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550406, nsv550409, nsv550408, nsv550407
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1035n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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