A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134067



Internal ID19284191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:124404402..124404488hg38UCSC Ensembl
Outerchr10:126092971..126093057hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv530n106
Supporting Variantsnssv3970406
SamplesKWS2
Known GenesOAT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134067
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