A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1034n54



Internal ID20134458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35600599..35673959hg38UCSC Ensembl
chr10:35889527..35962887hg19UCSC Ensembl
chr10:35929533..36002893hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3873361
hg1973361
hg1873361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550404, nsv550405
Samples1780862275_A, 1780862415_A
Known GenesFZD8, GJD4, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1034n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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