A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1577



Internal ID15546140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:78547626..78592890hg38UCSC Ensembl
Outerchr1:79013311..79058575hg19UCSC Ensembl
Outerchr1:78785899..78831163hg18UCSC Ensembl
Outerchr1:78725332..78770596hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3845265
hg1945265
hg1845265
hg1745265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5680
SamplesNA19129
Known Genes
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)nsv1577
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