A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660009



Internal ID15049975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68937355..69015325hg38UCSC Ensembl
Innerchr10:70697111..70775081hg19UCSC Ensembl
Innerchr10:70367117..70445087hg18UCSC Ensembl
Innerchr10:70367117..70445087hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3877971
hg1977971
hg1877971
hg1777971
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519999
Supporting Variants
Samples
Known GenesDDX21, DDX50, KIAA1279
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660009
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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