A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065588



Internal ID18808119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59207209..59244580hg38UCSC Ensembl
Innerchr18:56874441..56911812hg19UCSC Ensembl
Innerchr18:55025421..55062792hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3837372
hg1937372
hg1837372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565491
Samples
Known GenesGRP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065588
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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