A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7358



Internal ID15189820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:89980563..90025455hg38UCSC Ensembl
Outerchr1:90446122..90491014hg19UCSC Ensembl
Outerchr1:90218710..90263602hg18UCSC Ensembl
Outerchr1:90158143..90203035hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3844893
hg1944893
hg1844893
hg1744893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1843
Supporting Variants
SamplesNA12156
Known GenesGEMIN8P4, ZNF326
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)nssv7358
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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