A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10482n54



Internal ID22778377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32017441..32042495hg38UCSC Ensembl
chr6:31985218..32010272hg19UCSC Ensembl
chr6:32093196..32118251hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3825055
hg1925055
hg1825056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602093, nsv602081
Samples
Known GenesC4A, C4B, C4B_2, CYP21A2, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10482n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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