A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130645



Internal ID18927302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26710091..26713240hg38UCSC Ensembl
Outerchr10:26999020..27002169hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383150
hg193150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv382n106
Supporting Variantsnssv3966960
SamplesKWS2
Known GenesPDSS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130645
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