A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001111



Internal ID18743642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186796249..187014891hg38UCSC Ensembl
Innerchr3:186514038..186732679hg19UCSC Ensembl
Innerchr3:187996732..188215373hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38218643
hg19218642
hg18218642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615034
Samples
Known GenesADIPOQ, ADIPOQ-AS1, RFC4, ST6GAL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001111
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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