A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4721



Internal ID15196587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:155686903..155701781hg38UCSC Ensembl
Outerchr1:155656694..155671572hg19UCSC Ensembl
Outerchr1:153923318..153938196hg18UCSC Ensembl
Outerchr1:152469767..152484645hg17UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3814879
hg1914879
hg1814879
hg1714879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3054
Supporting Variants
SamplesNA19129
Known GenesDAP3, YY1AP1
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)nssv4721
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