A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119872



Internal ID19268998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:42821738..42821790hg38UCSC Ensembl
Outerchr11:42843288..42843340hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv627n106
Supporting Variantsnssv3982846
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119872
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