A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7405



Internal ID15536459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:58811578..58819024hg38UCSC Ensembl
Outerchr18:56478810..56486256hg19UCSC Ensembl
Outerchr18:54629790..54637236hg18UCSC Ensembl
Outerchr18:54629790..54637236hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg387447
hg197447
hg187447
hg177447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2324
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)nssv7405
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