A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059110



Internal ID18801641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10142986..10596015hg38UCSC Ensembl
Innerchr18:10142983..10596012hg19UCSC Ensembl
Innerchr18:10132983..10586012hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38453030
hg19453030
hg18453030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564101
Samples
Known GenesAPCDD1, NAPG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059110
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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