A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832557



Internal ID6158281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:20484575..20656055hg19UCSC Ensembl
Outerchr13:19382575..19554055hg18UCSC Ensembl
Outerchr13:19382575..19554055hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1450104
Samples
Known GenesZMYM2
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832557
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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