A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1321n54



Internal ID22769216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86653555..86682683hg38UCSC Ensembl
chr10:88413312..88442440hg19UCSC Ensembl
chr10:88403292..88432420hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3829129
hg1929129
hg1829129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551793, nsv551785
SamplesHGDP00619, HGDP00546
Known GenesLDB3, OPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1321n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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