A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576893



Internal ID16017616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:50801445..50819312hg38UCSC Ensembl
Innerchr18:48327815..48345682hg19UCSC Ensembl
Innerchr18:46581813..46599680hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3817868
hg1917868
hg1817868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv883093
Samples
Known GenesMRO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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