A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10839n54



Internal ID22778734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92289198..92366965hg38UCSC Ensembl
chr6:92998916..93076683hg19UCSC Ensembl
chr6:93055637..93133404hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3877768
hg1977768
hg1877768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604143, nsv604142, nsv604141
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10839n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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