A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055190



Internal ID19144409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14062273..14304890hg38UCSC Ensembl
Innerchr18:14062272..14304889hg19UCSC Ensembl
Innerchr18:14052272..14294889hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38242618
hg19242618
hg18242618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3321n100
Supporting Variantsnssv3564111
Samples
Known GenesANKRD20A5P, ZNF519
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055190
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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