A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10896n54



Internal ID22778791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107114286..107115095hg38UCSC Ensembl
chr6:107435490..107436299hg19UCSC Ensembl
chr6:107542183..107542992hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38810
hg19810
hg18810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604442, nsv604443, nsv604446
Samples
Known GenesBEND3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10896n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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