A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600788



Internal ID16041511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:666450..667538hg38UCSC Ensembl
Innerchr6:666450..667538hg19UCSC Ensembl
Innerchr6:611450..612538hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381089
hg191089
hg181089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10267n54
Supporting Variantsnssv1047616
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600788
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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