A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10251



Internal ID15542547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:166987472..167014235hg38UCSC Ensembl
Outerchr2:167843982..167870745hg19UCSC Ensembl
Outerchr2:167552228..167578991hg18UCSC Ensembl
Outerchr2:167669489..167696252hg17UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3826764
hg1926764
hg1826764
hg1726764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3019
Supporting Variants
SamplesNA18956
Known GenesXIRP2
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)nssv10251
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