A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833335



Internal ID6159059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:1617249..1731138hg19UCSC Ensembl
Outerchr17:1563999..1677888hg18UCSC Ensembl
Outerchr17:1563999..1677888hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain+Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1453052, nssv1453051
Samples
Known GenesMIR22, MIR22HG, SERPINF1, SERPINF2, SMYD4, WDR81
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833335
Frequency
Sample Size95
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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