A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018984



Internal ID19108201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5144960..5200567hg38UCSC Ensembl
Innerchr6:5145194..5200801hg19UCSC Ensembl
Innerchr6:5090193..5145800hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3855608
hg1955608
hg1855608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5913n100
Supporting Variantsnssv3747907
Samples
Known GenesLYRM4, MIR3691
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018984
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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