A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951170



Internal ID16953357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87347117..87353144hg38UCSC Ensembl
Outerchr9:46439401..46446900hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386028
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999479
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951170
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