A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016278



Internal ID19105497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:356103..384097hg38UCSC Ensembl
Innerchr6:356103..384097hg19UCSC Ensembl
Innerchr6:301103..329097hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3827995
hg1927995
hg1827995
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5906n100
Supporting Variantsnssv3654697, nssv3654695, nssv3654694, nssv3654696
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)nsv1016278
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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