A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963731



Internal ID19211861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:102474858..102474939hg38UCSC Ensembl
Outerchr10:104234615..104234696hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129499
Supporting Variants
SamplesKWS1
Known GenesTMEM180
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963731
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