A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604511



Internal ID16045234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110249364..110249531hg38UCSC Ensembl
Innerchr6:110570567..110570734hg19UCSC Ensembl
Innerchr6:110677260..110677427hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38168
hg19168
hg18168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072046
Samples
Known GenesMETTL24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604511
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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