A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033432



Internal ID18775966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26681909..26799954hg19UCSC Ensembl
Innerchr6:26789888..26907933hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg19118046
hg18118046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5929n100
Supporting Variantsnssv3654860
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)nsv1033432
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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