A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058002



Internal ID19147221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42476592..42496820hg38UCSC Ensembl
Innerchr18:40056557..40076785hg19UCSC Ensembl
Innerchr18:38310555..38330783hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3820229
hg1920229
hg1820229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565360
Samples
Known GenesLINC00907
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058002
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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