A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603107



Internal ID16043830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52748261..52792754hg38UCSC Ensembl
Innerchr6:52613059..52657552hg19UCSC Ensembl
Innerchr6:52721018..52765511hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3844494
hg1944494
hg1844494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10661n54
Supporting Variantsnssv1059614
Samples
Known GenesGSTA1, GSTA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603107
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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