A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956131



Internal ID17305004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:16332298..16332415hg38UCSC Ensembl
Outerchr9:16332296..16332413hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002402
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956131
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