A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577886



Internal ID16018609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79521227..79522270hg38UCSC Ensembl
Innerchr18:77281227..77282270hg19UCSC Ensembl
Innerchr18:75382215..75383258hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381044
hg191044
hg181044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv889150
Samples
Known GenesNFATC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer