A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517880



Internal ID15098487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:47810585..47855975hg38UCSC Ensembl
Innerchr17:45887951..45933341hg19UCSC Ensembl
Innerchr17:43242950..43288340hg18UCSC Ensembl
Innerchr17:43242950..43288340hg17UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3845391
hg1945391
hg1845391
hg1745391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695288
Samples
Known GenesLRRC46, MRPL10, OSBPL7, SCRN2, SP6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517880
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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