A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10925n54



Internal ID22778820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125855544..125865498hg38UCSC Ensembl
chr6:126176690..126186644hg19UCSC Ensembl
chr6:126218383..126228337hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg389955
hg199955
hg189955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604603, nsv604602
Samples
Known GenesNCOA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10925n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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