A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952926



Internal ID17301800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14353544..14354543hg38UCSC Ensembl
Outerchr16:14447401..14448400hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999224
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952926
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