A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521627



Internal ID15448920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:927869..933391hg38UCSC Ensembl
Innerchr17:831109..836631hg19UCSC Ensembl
Innerchr17:777859..783381hg18UCSC Ensembl
Innerchr17:777859..783381hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg385523
hg195523
hg185523
hg175523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698246
Samples
Known GenesNXN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521627
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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