A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605199



Internal ID16045922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163413723..163415657hg38UCSC Ensembl
Innerchr6:163834755..163836689hg19UCSC Ensembl
Innerchr6:163754745..163756679hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381935
hg191935
hg181935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11026n54
Supporting Variantsnssv1075602
Samples
Known GenesCAHM, QKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605199
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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