A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517219



Internal ID15444512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120909696..120923297hg38UCSC Ensembl
Innerchr10:122669208..122682809hg19UCSC Ensembl
Innerchr10:122659198..122672799hg18UCSC Ensembl
Innerchr10:122659198..122672799hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3813602
hg1913602
hg1813602
hg1713602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682860, nssv672725, nssv670814, nssv654045
Samples
Known GenesMIR5694
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517219
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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