A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576396



Internal ID16363805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:6487466..6522757hg38UCSC Ensembl
Innerchr18:6487465..6522756hg19UCSC Ensembl
Innerchr18:6477465..6512756hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3835292
hg1935292
hg1835292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877981
Samples
Known GenesC18orf64
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576396
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