A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059409



Internal ID19148628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42131135..42559481hg38UCSC Ensembl
Innerchr18:39711099..40139446hg19UCSC Ensembl
Innerchr18:37965097..38393444hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38428347
hg19428348
hg18428348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565351
Samples
Known GenesLINC00907
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059409
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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