A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031522



Internal ID18774056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60351931..60649461hg38UCSC Ensembl
Innerchr6:57323779..57617208hg19UCSC Ensembl
Innerchr6:57431738..57725167hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38297531
hg19293430
hg18293430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5969n100
Supporting Variantsnssv3745497, nssv3745498
Samples
Known GenesPRIM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031522
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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