A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958996



Internal ID19221338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133774775..133787422hg38UCSC Ensembl
Outerchr10:135512100..135524800hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3812648
hg1912701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118487
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958996
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