A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523906



Internal ID15451199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161509955..161530340hg38UCSC Ensembl
Innerchr1:161479745..161500130hg19UCSC Ensembl
Innerchr1:159746369..159766754hg18UCSC Ensembl
Innerchr1:158292800..158313185hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3820386
hg1920386
hg1820386
hg1720386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv17n21
Supporting Variantsnssv699749
Samples
Known GenesFCGR2A, HSPA6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523906
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