A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026543



Internal ID18769075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160306836..161585804hg38UCSC Ensembl
Innerchr6:160727868..162006836hg19UCSC Ensembl
Innerchr6:160647858..161926826hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381278969
hg191278969
hg181278969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654494
Samples
Known GenesAGPAT4, AGPAT4-IT1, LPA, LPAL2, MAP3K4, PARK2, PLG, SLC22A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026543
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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