A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516114



Internal ID15096721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128091905..128105538hg38UCSC Ensembl
Innerchr10:129890169..129903802hg19UCSC Ensembl
Innerchr10:129780159..129793792hg18UCSC Ensembl
Innerchr10:129780159..129793792hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3813634
hg1913634
hg1813634
hg1713634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv52n21
Supporting Variantsnssv666293, nssv703200, nssv678582, nssv696021
Samples
Known GenesMKI67
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516114
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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