A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv660n54



Internal ID20134084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182808616..182812684hg38UCSC Ensembl
chr1:182777751..182781819hg19UCSC Ensembl
chr1:181044374..181048442hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg384069
hg194069
hg184069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv548366, nsv548371, nsv548368, nsv548367, nsv548372, nsv548369
Samples
Known GenesNPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv660n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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