A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577882



Internal ID16018605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79467476..79528806hg38UCSC Ensembl
Innerchr18:77227476..77288806hg19UCSC Ensembl
Innerchr18:75328464..75389794hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3861331
hg1961331
hg1861331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv889146
Samples
Known GenesNFATC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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