A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1369n54



Internal ID20134793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97355926..97414113hg38UCSC Ensembl
chr10:99115683..99173870hg19UCSC Ensembl
chr10:99105673..99163860hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3858188
hg1958188
hg1858188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552024, nsv552023
Samples1780862019_A, HGDP01060
Known GenesRRP12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1369n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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