A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577562



Internal ID16018285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70286485..70293189hg38UCSC Ensembl
Innerchr18:67953721..67960425hg19UCSC Ensembl
Innerchr18:66104701..66111405hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg386705
hg196705
hg186705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6061n54
Supporting Variantsnssv887189
Samples
Known GenesSOCS6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577562
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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