A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602913



Internal ID16043636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35490065..35497645hg38UCSC Ensembl
Innerchr6:35457842..35465422hg19UCSC Ensembl
Innerchr6:35565820..35573400hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg387581
hg197581
hg187581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10624n54
Supporting Variantsnssv1058201
Samples
Known GenesTEAD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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