A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706096



Internal ID15096062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93680529..93711581hg38UCSC Ensembl
Innerchr10:95440286..95471338hg19UCSC Ensembl
Innerchr10:95430276..95461328hg18UCSC Ensembl
Innerchr10:95430276..95461328hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3831053
hg1931053
hg1831053
hg1731053
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522686
Supporting Variants
Samples
Known GenesFRA10AC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706096
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