A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525609



Internal ID15106216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120844479..120877218hg38UCSC Ensembl
Innerchr10:122603991..122636730hg19UCSC Ensembl
Innerchr10:122593981..122626720hg18UCSC Ensembl
Innerchr10:122593981..122626720hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3832740
hg1932740
hg1832740
hg1732740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701754
Samples
Known GenesMIR5694, WDR11, WDR11-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525609
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