A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv870n54



Internal ID22768765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238897660..238931547hg38UCSC Ensembl
chr1:239060960..239094847hg19UCSC Ensembl
chr1:237127583..237161470hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3833888
hg1933888
hg1833888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549430, nsv549431
SamplesHGDP00326, HGDP00321
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv870n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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