A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959446



Internal ID18870233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:79704044..79711544hg38UCSC Ensembl
Outerchr10:81463800..81471300hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387501
hg197501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110179
Supporting Variants
SamplesKWS1
Known GenesNUTM2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959446
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