A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10780n54



Internal ID22778675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74122408..74126569hg38UCSC Ensembl
chr6:74832124..74836285hg19UCSC Ensembl
chr6:74888844..74893005hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg384162
hg194162
hg184162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603758, nsv603751, nsv603755, nsv603746
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10780n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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