A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577809



Internal ID16018532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78979558..78980872hg38UCSC Ensembl
Innerchr18:76739558..76740872hg19UCSC Ensembl
Innerchr18:74840546..74841860hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381315
hg191315
hg181315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6101n54
Supporting Variantsnssv888864, nssv888870, nssv888866, nssv888863, nssv888868, nssv888867, nssv888865, nssv888869
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577809
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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