A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600669



Internal ID16041392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180604131..180642852hg38UCSC Ensembl
Innerchr5:180031131..180069852hg19UCSC Ensembl
Innerchr5:179963737..180002458hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3838722
hg1938722
hg1838722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153620
Samples1780862300_A
Known GenesFLT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600669
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