A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121103



Internal ID19256800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:126417903..126418217hg38UCSC Ensembl
Outerchr10:128106472..128106786hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv534n106
Supporting Variantsnssv3966223, nssv3963502
SamplesKWS2, KWS1
Known GenesLINC00601
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121103
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