A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7653



Internal ID15536211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:10140951..10165084hg38UCSC Ensembl
Outerchr20:10121599..10145732hg19UCSC Ensembl
Outerchr20:10069599..10093732hg18UCSC Ensembl
Outerchr20:10069599..10093732hg17UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3824134
hg1924134
hg1824134
hg1724134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3289
Supporting Variants
SamplesNA12156
Known GenesSNAP25-AS1
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)nssv7653
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