A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549038



Internal ID15989761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:203954701..204046590hg38UCSC Ensembl
Innerchr1:203923829..204015718hg19UCSC Ensembl
Innerchr1:202190452..202282341hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3891890
hg1991890
hg1891890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv734939
Samples
Known GenesLINC00303
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549038
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