A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020737



Internal ID19109955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60482050..60731785hg38UCSC Ensembl
Innerchr6:57449797..57699532hg19UCSC Ensembl
Innerchr6:57557756..57807491hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38249736
hg19249736
hg18249736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5970n100
Supporting Variantsnssv3657515
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)nsv1020737
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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