A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060440



Internal ID18802971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5208895..5321716hg38UCSC Ensembl
Innerchr18:5208894..5321715hg19UCSC Ensembl
Innerchr18:5198894..5311715hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38112822
hg19112822
hg18112822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725278
Samples
Known GenesLINC00526, LINC00667, ZBTB14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060440
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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