A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698246



Internal ID15434898
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 StatusS
Merged Variantsnsv521627
Supporting Variants
Samples
Known GenesNXN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698246
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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