A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832984



Internal ID6158708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:40794391..40998535hg19UCSC Ensembl
Outerchr15:38581683..38785827hg18UCSC Ensembl
Outerchr15:38581683..38785827hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1451923, nssv1451922
Samples
Known GenesC15orf57, CASC5, LOC100505648, MRPL42P5, RAD51, RPUSD2
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832984
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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