A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10638n54



Internal ID22778533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41734381..41735464hg38UCSC Ensembl
chr6:41702119..41703202hg19UCSC Ensembl
chr6:41810097..41811180hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381084
hg191084
hg181084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602986, nsv602983, nsv602985, nsv602984
Samples
Known GenesTFEB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10638n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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