A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576555



Internal ID16363964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15382822..15409414hg38UCSC Ensembl
Innerchr18:15382821..15409413hg19UCSC Ensembl
Innerchr18:15372821..15399413hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3826593
hg1926593
hg1826593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5870n54
Supporting Variantsnssv878479
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576555
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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