A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150704



Internal ID19200898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:71387756..71387826hg38UCSC Ensembl
Outerchr11:71098802..71098872hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996181
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150704
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