A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577814



Internal ID16365223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78979641..78980976hg38UCSC Ensembl
Innerchr18:76739641..76740976hg19UCSC Ensembl
Innerchr18:74840629..74841964hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381336
hg191336
hg181336
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6102n54
Supporting Variantsnssv888893, nssv888889, nssv888887, nssv888891, nssv888886, nssv888885, nssv888888, nssv888892, nssv888890
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577814
Frequency
Sample Size17421
Observed Gain6
Observed Loss3
Observed Complex0
Frequencyn/a


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