A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018829



Internal ID19108046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64996668..65167652hg38UCSC Ensembl
Innerchr6:65706561..65877545hg19UCSC Ensembl
Innerchr6:65763282..65934266hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38170985
hg19170985
hg18170985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5998n100
Supporting Variantsnssv3657657, nssv3657658
Samples
Known GenesEYS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018829
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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