A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999166



Internal ID17292118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:88549270..88554869hg38UCSC Ensembl
Outerchr15:89092501..89098100hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952022
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999166
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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