A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027292



Internal ID18769824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57361384..60592382hg38UCSC Ensembl
Innerchr6:57226182..57560129hg19UCSC Ensembl
Innerchr6:57334141..57668088hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383230999
hg19333948
hg18333948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5967n100
Supporting Variantsnssv3657505
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)nsv1027292
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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