A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605203



Internal ID16045926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163413825..163415602hg38UCSC Ensembl
Innerchr6:163834857..163836634hg19UCSC Ensembl
Innerchr6:163754847..163756624hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381778
hg191778
hg181778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11026n54
Supporting Variantsnssv1075606, nssv1075608, nssv1075607
Samples
Known GenesCAHM, QKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605203
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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