A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688667



Internal ID15078633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:407430..410932hg38UCSC Ensembl
Innerchr5:407545..411047hg19UCSC Ensembl
Innerchr5:460545..464047hg18UCSC Ensembl
Innerchr5:460545..464047hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg383503
hg193503
hg183503
hg173503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516539
Supporting Variants
Samples
Known GenesAHRR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688667
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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