A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521859



Internal ID15449152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106227944..106255743hg38UCSC Ensembl
Innerchr6:106675819..106703618hg19UCSC Ensembl
Innerchr6:106782512..106810311hg18UCSC Ensembl
Innerchr6:106782512..106810311hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3827800
hg1927800
hg1827800
hg1727800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv391n21
Supporting Variantsnssv694633
Samples
Known GenesATG5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521859
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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