A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058132



Internal ID19147351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:38788882..38812203hg38UCSC Ensembl
Innerchr19:39279522..39302843hg19UCSC Ensembl
Innerchr19:43971362..43994683hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823322
hg1923322
hg1823322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724536
Samples
Known GenesLGALS4, LGALS7B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058132
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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