A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576316



Internal ID16017039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3680476..3736629hg38UCSC Ensembl
Innerchr18:3680476..3736629hg19UCSC Ensembl
Innerchr18:3670476..3726629hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3856154
hg1956154
hg1856154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877424
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576316
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