A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121088



Internal ID18921503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1495596..1495703hg38UCSC Ensembl
Outerchr10:1537791..1537898hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv336n106
Supporting Variantsnssv3964304, nssv3962067
SamplesKWS2, KWS1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121088
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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