A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577877



Internal ID16018600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79388973..79404443hg38UCSC Ensembl
Innerchr18:77148973..77164443hg19UCSC Ensembl
Innerchr18:75249961..75265431hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3815471
hg1915471
hg1815471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv889142
Samples
Known GenesNFATC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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