A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958932



Internal ID18866777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:3336136..3337336hg38UCSC Ensembl
Outerchr1:3252700..3253900hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118426
Supporting Variants
SamplesKWS1
Known GenesPRDM16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958932
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