A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10268n54



Internal ID20143692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:666450..667756hg38UCSC Ensembl
chr6:666450..667756hg19UCSC Ensembl
chr6:611450..612756hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381307
hg191307
hg181307
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600792, nsv600795, nsv600790
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10268n54
Frequency
Sample Size17421
Observed Gain33
Observed Loss847
Observed Complex0
Frequencyn/a


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