A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700086



Internal ID15090052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189310262..189354225hg38UCSC Ensembl
Innerchr4:190231416..190275379hg19UCSC Ensembl
Innerchr4:190468410..190512373hg18UCSC Ensembl
Innerchr4:190606565..190650528hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3843964
hg1943964
hg1843964
hg1743964
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)nssv700086
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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