A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016229



Internal ID19105448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:81012514..81171356hg38UCSC Ensembl
Innerchr6:81722231..81881073hg19UCSC Ensembl
Innerchr6:81778950..81937792hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38158843
hg19158843
hg18158843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3750115
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)nsv1016229
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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