A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577804



Internal ID16018527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78979457..78980923hg38UCSC Ensembl
Innerchr18:76739457..76740923hg19UCSC Ensembl
Innerchr18:74840445..74841911hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381467
hg191467
hg181467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6101n54
Supporting Variantsnssv888845, nssv888844
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577804
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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