A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109034



Internal ID19248001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88229570..88229667hg38UCSC Ensembl
Outerchr16:88263176..88263273hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954868
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109034
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