A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9594



Internal ID15539720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:7091241..7134851hg38UCSC Ensembl
Outerchr20:7071888..7115498hg19UCSC Ensembl
Outerchr20:7019888..7063498hg18UCSC Ensembl
Outerchr20:7019888..7063498hg17UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3843611
hg1943611
hg1843611
hg1743611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3277
Supporting Variants
SamplesNA18507
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)nssv9594
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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