A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547651



Internal ID15988374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:144946566..145023143hg38UCSC Ensembl
Innerchr1:143964483..144062541hg19UCSC Ensembl
Innerchr1:142675840..142773898hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3876578
hg1998059
hg1898059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv723055
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547651
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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