A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10757n54



Internal ID22778652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69036162..69084187hg38UCSC Ensembl
chr6:69746054..69794079hg19UCSC Ensembl
chr6:69802775..69850800hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3848026
hg1948026
hg1848026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603632, nsv603633
SamplesHGDP00635
Known GenesBAI3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10757n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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