A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769339



Internal ID18967076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57340901..57420102hg38UCSC Ensembl
chr6:57205699..57284900hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg3879202
hg1979202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077472
Supporting Variants
SamplesKWP1
Known GenesPRIM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769339
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer