A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138667



Internal ID19280194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9825502..9825575hg38UCSC Ensembl
Outerchr19:9936178..9936251hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991250
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138667
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