A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067095



Internal ID19156314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:64442723..64590176hg38UCSC Ensembl
Innerchr18:62109958..62257411hg19UCSC Ensembl
Innerchr18:60260938..60408391hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38147454
hg19147454
hg18147454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3378n100
Supporting Variantsnssv3726095
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)nsv1067095
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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