A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670786



Internal ID15060752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189295710..189369306hg38UCSC Ensembl
Innerchr4:190216864..190290460hg19UCSC Ensembl
Innerchr4:190453858..190527454hg18UCSC Ensembl
Innerchr4:190592013..190665609hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3873597
hg1973597
hg1873597
hg1773597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517295
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670786
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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