A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577883



Internal ID16018606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79481665..79516964hg38UCSC Ensembl
Innerchr18:77241665..77276964hg19UCSC Ensembl
Innerchr18:75342653..75377952hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3835300
hg1935300
hg1835300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6113n54
Supporting Variantsnssv889147
Samples
Known GenesNFATC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577883
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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