A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056192



Internal ID19145411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42460509..42478430hg38UCSC Ensembl
Innerchr18:40040474..40058395hg19UCSC Ensembl
Innerchr18:38294472..38312393hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3817922
hg1917922
hg1817922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3344n100
Supporting Variantsnssv3565353, nssv3565356, nssv3565355, nssv3565354
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)nsv1056192
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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