A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017886



Internal ID19107103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103317795..104262881hg38UCSC Ensembl
Innerchr6:103765670..104710756hg19UCSC Ensembl
Innerchr6:103872363..104817449hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38945087
hg19945087
hg18945087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3653501
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)nsv1017886
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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