A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976446



Internal ID19240779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:59330640..59333040hg38UCSC Ensembl
Outerchr10:61090400..61092800hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382401
hg192401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115395
Supporting Variants
SamplesKWS2
Known GenesFAM13C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976446
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