A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695359



Internal ID15432011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141849315..141874340hg38UCSC Ensembl
Innerchr4:142770468..142795493hg19UCSC Ensembl
Innerchr4:142989918..143014943hg18UCSC Ensembl
Innerchr4:143128073..143153098hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3825026
hg1925026
hg1825026
hg1725026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517947
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695359
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer