A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576394



Internal ID16363803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5950154..5967910hg38UCSC Ensembl
Innerchr18:5950153..5967909hg19UCSC Ensembl
Innerchr18:5940153..5957909hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3817757
hg1917757
hg1817757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877979
Samples
Known GenesL3MBTL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576394
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