A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115724



Internal ID19249514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:112629698..112638598hg38UCSC Ensembl
Outerchr6:112950900..112959800hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg388901
hg198901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977532
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115724
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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