A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016123



Internal ID19105341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..217536hg38UCSC Ensembl
Innerchr6:149649..217536hg19UCSC Ensembl
Innerchr6:94649..162536hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3867888
hg1967888
hg1867888
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3650363, nssv3746762
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)nsv1016123
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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