A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119828



Internal ID19255535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76577013..76577087hg38UCSC Ensembl
Outerchr10:78336771..78336845hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982782
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119828
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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