A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8821



Internal ID15188357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24165623..24199731hg38UCSC Ensembl
Outerchr1:24492113..24526221hg19UCSC Ensembl
Outerchr1:24364700..24398808hg18UCSC Ensembl
Outerchr1:24237419..24271527hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385329
hg195329
hg185329
hg175329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6853
Supporting Variants
SamplesNA12156
Known GenesIFNLR1
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)nssv8821
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