A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067174



Internal ID19156393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:51202320..51238569hg38UCSC Ensembl
Innerchr18:48728690..48764939hg19UCSC Ensembl
Innerchr18:46982688..47018937hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3836250
hg1936250
hg1836250
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3356n100
Supporting Variantsnssv3565446
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)nsv1067174
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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