A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951994



Internal ID16954181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74614960..74633959hg38UCSC Ensembl
Outerchr15:74907301..74926300hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3819000
hg1919000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999135
SamplesBILGI_BIOE
Known GenesCLK3, EDC3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951994
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer