A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576736



Internal ID16364145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42462042..42477560hg38UCSC Ensembl
Innerchr18:40042007..40057525hg19UCSC Ensembl
Innerchr18:38296005..38311523hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3815519
hg1915519
hg1815519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv882313
Samples
Known GenesLINC00907
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576736
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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