A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664497



Internal ID15401149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126837454..126925273hg38UCSC Ensembl
Innerchr10:128526023..128613842hg19UCSC Ensembl
Innerchr10:128516013..128603832hg18UCSC Ensembl
Innerchr10:128516013..128603832hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3887820
hg1987820
hg1887820
hg1787820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515706
Supporting Variants
Samples
Known GenesDOCK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664497
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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