A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018678



Internal ID19107895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65106986..65157876hg38UCSC Ensembl
Innerchr6:65816879..65867769hg19UCSC Ensembl
Innerchr6:65873600..65924490hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3850891
hg1950891
hg1850891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657662
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)nsv1018678
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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