A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137632



Internal ID19253000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39364803..39398103hg38UCSC Ensembl
Outerchr9:39364800..39398100hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3833301
hg1933301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990133
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137632
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer