A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951968



Internal ID17300842
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 StatusM
Merged Variants
Supporting Variantsnssv2999107
SamplesBILGI_BIOE
Known GenesFOXB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951968
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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