A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146274



Internal ID18852637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15149222..15149299hg38UCSC Ensembl
Outerchr10:15191221..15191298hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999478
SamplesKWB1
Known GenesNMT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146274
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer