A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577429



Internal ID16364838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69078971..69100794hg38UCSC Ensembl
Innerchr18:66746208..66768031hg19UCSC Ensembl
Innerchr18:64897188..64919011hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3821824
hg1921824
hg1821824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886729, nssv886728
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577429
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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