A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577811



Internal ID16365220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78979558..78980976hg38UCSC Ensembl
Innerchr18:76739558..76740976hg19UCSC Ensembl
Innerchr18:74840546..74841964hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381419
hg191419
hg181419
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6102n54
Supporting Variantsnssv888878, nssv888877, nssv888879, nssv888875, nssv888876, nssv888880, nssv888882, nssv888874, nssv888881, nssv888873
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577811
Frequency
Sample Size17421
Observed Gain7
Observed Loss3
Observed Complex0
Frequencyn/a


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