A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577089



Internal ID16364498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62522582..62528636hg38UCSC Ensembl
Innerchr18:60189815..60195869hg19UCSC Ensembl
Innerchr18:58340795..58346849hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg386055
hg196055
hg186055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv884988
Samples
Known GenesZCCHC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577089
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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