A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516718



Internal ID15444011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117448658..117450864hg38UCSC Ensembl
Innerchr10:119208169..119210375hg19UCSC Ensembl
Innerchr10:119198159..119200365hg18UCSC Ensembl
Innerchr10:119198159..119200365hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382207
hg192207
hg182207
hg172207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663274, nssv670431
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516718
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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