A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769405



Internal ID18967583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10428900..10442301hg38UCSC Ensembl
chr12:10581499..10594900hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3813402
hg1913402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070507
Supporting Variants
SamplesKWP1
Known GenesKLRC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769405
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