A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978312



Internal ID19245717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40769572..40833272hg38UCSC Ensembl
Outerchr9:66722600..66786300hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3863701
hg1963701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139976
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978312
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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