A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1327n54



Internal ID22769222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86942473..86943239hg38UCSC Ensembl
chr10:88702230..88702996hg19UCSC Ensembl
chr10:88692210..88692976hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38767
hg19767
hg18767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551808, nsv551807, nsv551799, nsv551805, nsv551802
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1327n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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