A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024902



Internal ID18767433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57361384..60800942hg38UCSC Ensembl
Innerchr6:57226182..57768689hg19UCSC Ensembl
Innerchr6:57334141..57876648hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383439559
hg19542508
hg18542508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5968n100
Supporting Variantsnssv3745495
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)nsv1024902
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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