A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600791



Internal ID16041514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:666450..667705hg38UCSC Ensembl
Innerchr6:666450..667705hg19UCSC Ensembl
Innerchr6:611450..612705hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381256
hg191256
hg181256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10269n54
Supporting Variantsnssv1047630, nssv1047628, nssv1047627, nssv1047632, nssv1047629, nssv1047626, nssv1047631
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600791
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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