A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10989n54



Internal ID22778884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160814066..160850745hg38UCSC Ensembl
chr6:161235098..161271777hg19UCSC Ensembl
chr6:161155088..161191767hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3836680
hg1936680
hg1836680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605006, nsv605007
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10989n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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