A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056187



Internal ID19145406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74390239..74406717hg38UCSC Ensembl
Innerchr18:72057474..72073952hg19UCSC Ensembl
Innerchr18:70208454..70224932hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3816479
hg1916479
hg1816479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3402n100
Supporting Variantsnssv3563008, nssv3563009
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056187
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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