A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1318n54



Internal ID22769213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86366077..86367652hg38UCSC Ensembl
chr10:88125834..88127409hg19UCSC Ensembl
chr10:88115814..88117389hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381576
hg191576
hg181576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551777, nsv551778, nsv551775, nsv551776
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1318n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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