A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576322



Internal ID16363731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4529974..4536648hg38UCSC Ensembl
Innerchr18:4529974..4536648hg19UCSC Ensembl
Innerchr18:4519974..4526648hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386675
hg196675
hg186675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5820n54
Supporting Variantsnssv877429, nssv877428, nssv877430
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576322
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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