A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703823



Internal ID15440475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:382993..460640hg38UCSC Ensembl
Innerchr8:332993..410640hg19UCSC Ensembl
Innerchr8:322993..400640hg18UCSC Ensembl
Innerchr8:322993..400640hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3877648
hg1977648
hg1877648
hg1777648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527388
Supporting Variants
Samples
Known GenesFAM87A, FBXO25
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703823
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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