A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7566n54



Internal ID22775461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37364924..37447464hg38UCSC Ensembl
chr20:35993327..36075866hg19UCSC Ensembl
chr20:35426741..35509280hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3882541
hg1982540
hg1882540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585959, nsv585958, nsv585957, nsv585960, nsv585961
SamplesHGDP00850, NINDS_51, HGDP00864, NINDS_136
Known GenesSRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7566n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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