A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577810



Internal ID16365219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78979558..78980923hg38UCSC Ensembl
Innerchr18:76739558..76740923hg19UCSC Ensembl
Innerchr18:74840546..74841911hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381366
hg191366
hg181366
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6102n54
Supporting Variantsnssv888872, nssv888871
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577810
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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