A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526106



Internal ID15106713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109098754..109104587hg38UCSC Ensembl
Innerchr12:109536559..109542392hg19UCSC Ensembl
Innerchr12:108020942..108026775hg18UCSC Ensembl
Innerchr12:107999279..108005112hg17UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg385834
hg195834
hg185834
hg175834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702354
Samples
Known GenesUNG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526106
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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