A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8064



Internal ID15189114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:10373216..10417961hg38UCSC Ensembl
Outerchr5:10373328..10418073hg19UCSC Ensembl
Outerchr5:10426328..10471073hg18UCSC Ensembl
Outerchr5:10426328..10471073hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3844746
hg1944746
hg1844746
hg1744746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4713
Supporting Variants
SamplesNA12156
Known GenesMARCH6
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)nssv8064
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