A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521009



Internal ID15101616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135394237..135400147hg38UCSC Ensembl
Innerchr6:135715375..135721285hg19UCSC Ensembl
Innerchr6:135757068..135762978hg18UCSC Ensembl
Innerchr6:135757068..135762978hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg385911
hg195911
hg185911
hg175911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679741, nssv687303
Samples
Known GenesAHI1, MIR548H4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521009
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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