A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768578



Internal ID18966227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159169367..159169668hg38UCSC Ensembl
chr6:159590399..159590700hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073603
Supporting Variants
SamplesKWP1
Known GenesFNDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768578
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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