A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600789



Internal ID16041512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:666450..667546hg38UCSC Ensembl
Innerchr6:666450..667546hg19UCSC Ensembl
Innerchr6:611450..612546hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381097
hg191097
hg181097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10267n54
Supporting Variantsnssv1047621, nssv1047617, nssv1047618, nssv1047620, nssv1047622, nssv1047619
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600789
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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