A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520329



Internal ID15447622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106236120..106255743hg38UCSC Ensembl
Innerchr6:106683995..106703618hg19UCSC Ensembl
Innerchr6:106790688..106810311hg18UCSC Ensembl
Innerchr6:106790688..106810311hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3819624
hg1919624
hg1819624
hg1719624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv391n21
Supporting Variantsnssv675241, nssv662951
Samples
Known GenesATG5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520329
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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