A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7210



Internal ID15189968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:86078294..86119577hg38UCSC Ensembl
Outerchr15:86621525..86662808hg19UCSC Ensembl
Outerchr15:84422529..84463812hg18UCSC Ensembl
Outerchr15:84422529..84463812hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3841284
hg1941284
hg1841284
hg1741284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1648
Supporting Variants
SamplesNA12156
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)nssv7210
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