A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015989



Internal ID19105207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65182487..65245398hg38UCSC Ensembl
Innerchr6:65892380..65955291hg19UCSC Ensembl
Innerchr6:65949101..66012012hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3862912
hg1962912
hg1862912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745569
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)nsv1015989
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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