A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125887



Internal ID19273694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:118940825..118941153hg38UCSC Ensembl
Outerchr6:119261990..119262318hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3964097, nssv3984093
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125887
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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