A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528028



Internal ID15108635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14400348..14563663hg38UCSC Ensembl
Innerchr10:14442347..14605662hg19UCSC Ensembl
Innerchr10:14482353..14645668hg18UCSC Ensembl
Innerchr10:14482353..14645668hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38163316
hg19163316
hg18163316
hg17163316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704557
Samples
Known GenesFAM107B, MIR1265
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528028
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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