A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016001



Internal ID18758536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110959208..110988298hg38UCSC Ensembl
Innerchr6:111280411..111309501hg19UCSC Ensembl
Innerchr6:111387104..111416194hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3829091
hg1929091
hg1829091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654296
Samples
Known GenesGTF3C6, RPF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016001
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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