A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7642n54



Internal ID22775537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61715436..61742162hg38UCSC Ensembl
chr20:60290492..60317218hg19UCSC Ensembl
chr20:59723887..59750613hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3826727
hg1926727
hg1826727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586442, nsv586441
SamplesHGDP00017, HGDP00341, HGDP00230
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7642n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer