A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521035



Internal ID15448328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:68372306..68420159hg38UCSC Ensembl
Innerchr12:68766086..68813939hg19UCSC Ensembl
Innerchr12:67052353..67100206hg18UCSC Ensembl
Innerchr12:67052353..67100206hg17UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3847854
hg1947854
hg1847854
hg1747854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697747
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521035
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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