A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152600



Internal ID19198576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:17899520..17902885hg38UCSC Ensembl
Outerchr9:17899518..17902883hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg383366
hg193366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999780
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152600
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