A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528680



Internal ID8422955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102886563..102911770hg38UCSC Ensembl
Innerchr4:103807720..103832927hg19UCSC Ensembl
Innerchr4:104027155..104052376hg18UCSC Ensembl
Innerchr4:104165310..104190531hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3825208
hg1925208
hg1825222
hg1725222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705321
Samples
Known GenesCISD2, SLC9B1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528680
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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