A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609



Internal ID15550435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:3960657..3997922hg38UCSC Ensembl
Outerchr10:4002849..4040114hg19UCSC Ensembl
Outerchr10:3992849..4030114hg18UCSC Ensembl
Outerchr10:3992849..4030114hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3837266
hg1937266
hg1837266
hg1737266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8379
SamplesNA12156
Known GenesMIR6078
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)nsv5609
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