A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065382



Internal ID18807913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11723231..11769733hg38UCSC Ensembl
Innerchr18:11723230..11769732hg19UCSC Ensembl
Innerchr18:11713230..11759732hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3846503
hg1946503
hg1846503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564103
Samples
Known GenesGNAL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065382
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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