A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2210



Internal ID15194807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9160648..9200494hg38UCSC Ensembl
Outerchr19:9271324..9311170hg19UCSC Ensembl
Outerchr19:9132324..9172170hg18UCSC Ensembl
Outerchr19:9132324..9172170hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839847
hg1939847
hg1839847
hg1739847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2411
Supporting Variants
SamplesNA18555
Known GenesOR7D2, ZNF317
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)nssv2210
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