A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604504



Internal ID16045227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110248622..110250090hg38UCSC Ensembl
Innerchr6:110569825..110571293hg19UCSC Ensembl
Innerchr6:110676518..110677986hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381469
hg191469
hg181469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10908n54
Supporting Variantsnssv1072012, nssv1072011
Samples
Known GenesMETTL24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604504
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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