A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058290



Internal ID18800821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58487122..58512805hg38UCSC Ensembl
Innerchr16:58521026..58546709hg19UCSC Ensembl
Innerchr16:57078527..57104210hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3825684
hg1925684
hg1825684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559362
Samples
Known GenesNDRG4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058290
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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