A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999107



Internal ID17292059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:59998802..60007001hg38UCSC Ensembl
Outerchr15:60291001..60299200hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951968
Supporting Variants
SamplesBILGI_BIOE
Known GenesFOXB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999107
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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