A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832973



Internal ID6158697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:38443805..38644882hg19UCSC Ensembl
Outerchr15:36231097..36432174hg18UCSC Ensembl
Outerchr15:36231097..36432174hg17UCSC Ensembl
Cytoband15q14
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 Variantsnssv1451908
Samples
Known GenesSPRED1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832973
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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