A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7626



Internal ID15552654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132060874..132088842hg38UCSC Ensembl
Outerchr10:133874378..133902346hg19UCSC Ensembl
Outerchr10:133724368..133752336hg18UCSC Ensembl
Outerchr10:133724368..133752336hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3827969
hg1927969
hg1827969
hg1727969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3909
SamplesNA12878
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)nsv7626
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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