A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952611



Internal ID16954798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:40237800..40284699hg38UCSC Ensembl
Outerchr15:40530001..40576900hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3846900
hg1946900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999078
SamplesBILGI_BIOE
Known GenesANKRD63, C15orf56, PAK6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952611
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