A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577652



Internal ID16365061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74415709..74462299hg38UCSC Ensembl
Innerchr18:72082944..72129534hg19UCSC Ensembl
Innerchr18:70233924..70280514hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3846591
hg1946591
hg1846591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887378
Samples
Known GenesFAM69C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577652
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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