A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055157



Internal ID19144376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:20961686..21024743hg38UCSC Ensembl
Innerchr18:18541647..18604704hg19UCSC Ensembl
Innerchr18:16795645..16858702hg18UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg3863058
hg1963058
hg1863058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3324n100
Supporting Variantsnssv3564127
Samples
Known GenesROCK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055157
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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