A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7667n54



Internal ID22775562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63522433..63576509hg38UCSC Ensembl
chr20:62153786..62207862hg19UCSC Ensembl
chr20:61624230..61678306hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3854077
hg1954077
hg1854077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586570, nsv586572
SamplesHGDP00696, NINDS_49
Known GenesC20orf195, HELZ2, PTK6, SRMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7667n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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