A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979920



Internal ID19246021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:96193439..96221337hg38UCSC Ensembl
Outerchr6:96641315..96669213hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3827899
hg1927899
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125883
Supporting Variants
SamplesKWS2
Known GenesFUT9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979920
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