A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016866



Internal ID19106083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103270306..103314174hg38UCSC Ensembl
Innerchr6:103718181..103762049hg19UCSC Ensembl
Innerchr6:103824874..103868742hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3843869
hg1943869
hg1843869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6118n100
Supporting Variantsnssv3649885
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016866
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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