A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030207



Internal ID19119426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..221515hg38UCSC Ensembl
Innerchr6:149649..221515hg19UCSC Ensembl
Innerchr6:94649..166515hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3871867
hg1971867
hg1871867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5866n100
Supporting Variantsnssv3746763
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)nsv1030207
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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