A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022863



Internal ID18765397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57946158..58060451hg38UCSC Ensembl
Innerchr6:58272436..58386729hg19UCSC Ensembl
Innerchr6:58380395..58494688hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38114294
hg19114294
hg18114294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5978n100
Supporting Variantsnssv3657555
Samples
Known GenesGUSBP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022863
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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