A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979520



Internal ID19240169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:8559422..8560126hg38UCSC Ensembl
Outerchr3:8601108..8601812hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117326
Supporting Variants
SamplesKWS2
Known GenesLMCD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979520
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