A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522889



Internal ID15103496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:171780525..171785931hg38UCSC Ensembl
Innerchr1:171749665..171755071hg19UCSC Ensembl
Innerchr1:170016288..170021694hg18UCSC Ensembl
Innerchr1:168481322..168486728hg17UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg385407
hg195407
hg185407
hg175407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698547
Samples
Known GenesMETTL13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522889
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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