A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359



Internal ID15204574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:116850402..116884438hg38UCSC Ensembl
Outerchr8:117862641..117896677hg19UCSC Ensembl
Outerchr8:117931822..117965858hg18UCSC Ensembl
Outerchr8:117931822..117965858hg17UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg385404
hg195404
hg185404
hg175404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8543
SamplesNA12156
Known GenesMIR3610, RAD21, RAD21-AS1
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)nsv6359
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