A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv888840



Internal ID15836110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78978993..78981423hg38UCSC Ensembl
Innerchr18:76738993..76741423hg19UCSC Ensembl
Innerchr18:74839981..74842411hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg382431
hg192431
hg182431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577800
Supporting Variants
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv888840
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