A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958799



Internal ID17307672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:24871783..24873496hg38UCSC Ensembl
Outerchr15:25116930..25118643hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381714
hg191714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005469
SamplesBILGI_BIOE
Known GenesSNRPN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958799
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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