A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951995



Internal ID17300869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75201760..75238159hg38UCSC Ensembl
Outerchr15:75494101..75530500hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3836400
hg1936400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999136
SamplesBILGI_BIOE
Known GenesC15orf39
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951995
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