A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576636



Internal ID16017359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31566859..31610211hg38UCSC Ensembl
Innerchr18:29146822..29190174hg19UCSC Ensembl
Innerchr18:27400820..27444172hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3843353
hg1943353
hg1843353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878945
Samples
Known GenesTTR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576636
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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