A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577795



Internal ID16018518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78972221..79050030hg38UCSC Ensembl
Innerchr18:76732221..76810030hg19UCSC Ensembl
Innerchr18:74833209..74911018hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3877810
hg1977810
hg1877810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv888832
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577795
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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