A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763590



Internal ID19309690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110092773..110093574hg38UCSC Ensembl
chr11:109963499..109964300hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070487
Supporting Variants
SamplesKWP1
Known GenesZC3H12C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763590
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