A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772805



Internal ID18962383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51310245..51312046hg38UCSC Ensembl
chr19:51813499..51815300hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071943
Supporting Variants
SamplesKWP1
Known GenesIGLON5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772805
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