A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056694



Internal ID19145913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42469073..42502702hg38UCSC Ensembl
Innerchr18:40049038..40082667hg19UCSC Ensembl
Innerchr18:38303036..38336665hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3833630
hg1933630
hg1833630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565359
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)nsv1056694
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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