A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772000



Internal ID18967472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12518459..12520974hg38UCSC Ensembl
chr10:12560458..12562973hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382516
hg192516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073741
Supporting Variants
SamplesKWP1
Known GenesCAMK1D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772000
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