A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10466n54



Internal ID20143890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31980320..32029165hg38UCSC Ensembl
chr6:31948097..31996942hg19UCSC Ensembl
chr6:32056076..32104920hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3848846
hg1948846
hg1848845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601994, nsv602010, nsv602031, nsv601992, nsv602009, nsv602025, nsv602006, nsv602005, nsv601993, nsv602023, nsv601974, nsv602007, nsv601973, nsv601995, nsv602008, nsv602024
Samples
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2, STK19, TNXA, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10466n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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