A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1324n54



Internal ID22769219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86942473..86942967hg38UCSC Ensembl
chr10:88702230..88702724hg19UCSC Ensembl
chr10:88692210..88692704hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38495
hg19495
hg18495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551803, nsv551796, nsv551801
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1324n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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