A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762492



Internal ID19311578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66499675..66503576hg38UCSC Ensembl
chr3:66550099..66554000hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074599
Supporting Variants
SamplesKWP1
Known GenesLRIG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762492
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