A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577874



Internal ID16018597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79339963..79398225hg38UCSC Ensembl
Innerchr18:77099963..77158225hg19UCSC Ensembl
Innerchr18:75200951..75259213hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3858263
hg1958263
hg1858263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv889139
Samples
Known GenesATP9B, NFATC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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