A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063769



Internal ID19152988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:20961686..21023903hg38UCSC Ensembl
Innerchr18:18541647..18603864hg19UCSC Ensembl
Innerchr18:16795645..16857862hg18UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg3862218
hg1962218
hg1862218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3324n100
Supporting Variantsnssv3564126
Samples
Known GenesROCK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063769
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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