A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7560



Internal ID15552582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:114004292..114034529hg38UCSC Ensembl
Outerchr10:115764051..115794288hg19UCSC Ensembl
Outerchr10:115754041..115784278hg18UCSC Ensembl
Outerchr10:115754041..115784278hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg389048
hg199048
hg189048
hg179048
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5320
SamplesNA19129
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7560
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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