A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072011



Internal ID15578511
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 StatusS
Merged Variantsnsv604504
Supporting Variants
Samples
Known GenesMETTL24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072011
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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