A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523985



Internal ID15104592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79467476..79490638hg38UCSC Ensembl
Innerchr18:77227476..77250638hg19UCSC Ensembl
Innerchr18:75328464..75351626hg18UCSC Ensembl
Innerchr18:75328464..75351626hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3823163
hg1923163
hg1823163
hg1723163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699841
Samples
Known GenesNFATC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523985
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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