A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061891



Internal ID18804422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4356108..4505125hg38UCSC Ensembl
Innerchr18:4356108..4505125hg19UCSC Ensembl
Innerchr18:4346108..4495125hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38149018
hg19149018
hg18149018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564072
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061891
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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